
Luneburger Schanze 26 SE DECISION MADE: 17-AUG-22Ģ1614 Buxtehude DE 510(k) SUMMARY AVAILABLE FROM FDAī&Medi Co., Ltd. Implantcast, GmbH 510(k) NO: K210678(Traditional)ĪTTN: Juliane Hoppner PHONE NO : 49 4161 7440 Taoyuan City TW 33377 510(k) SUMMARY AVAILABLE FROM FDA 188, Wenhua 2nd Road, Guishan SE DECISION MADE: 02-AUG-22
#Fda 510k database portable#
Huizhou CN 516005 510(k) SUMMARY AVAILABLE FROM FDAĭEVICE: QOCA Portable ECG Monitoring Device No.2 XingDe East Road, DongJiang HSE DECISION MADE: 19-AUG-22 HuiZhou TianChang Industrial Co., 510(k) NO: K203078(Abbreviated) Shenzhen CN 518116 510(k) SUMMARY AVAILABLE FROM FDAĭEVICE: CAREWE Surgical Face Mask Models N001-AW, N002-AW, and N003-AW A6B7 (Block G), ShangRong InduSE DECISION MADE: 12-AUG-22

510(k) NO: K202508(Traditional)ĪTTN: Keith Buchholz PHONE NO : 763 4228311ġ2297 Ensigh Avenue North SE DECISION MADE: 12-AUG-22Ĭhamplin MN 55316 510(k) SUMMARY AVAILABLE FROM FDAĭEVICE: Bioland G-425-2V Blood Glucose Monitoring System, Bioland G-425-2 Blood Glucose Monitoring Systemīioland Technology Ltd. Macon GA 31201 510(k) SUMMARY AVAILABLE FROM FDAĭi-Chem, Inc. Smisson-Cartledge Biomedical LLC 510(k) NO: K202461(Traditional)ĪTTN: Calder Clay III PHONE NO : 478 7449992Ĥ87 Cherry Street - Third Street TSE DECISION MADE: 12-AUG-22 Largo FL 33770 510(k) SUMMARY AVAILABLE FROM FDAĭEVICE: ThermaCor 1200 Disposable Sets for the ThermaCor 1200 Rapid Thermal Infusion System San Fernando CA 91340 510(k) SUMMARY AVAILABLE FROM FDAĭEVICE: Powered Inflatable Tube Massager - SLIM UP DRAINįoggiare Technologies LLC 510(k) NO: K201730(Traditional)ĪTTN: Thierry Germanovitch PHONE NO : 954 9998063ġ920 West Bay Drive, Suite 4 SE DECISION MADE: 22-AUG-22 Solidence Surgical Corporation 510(k) NO: K191131(Traditional)ġ104 San Fernando Road SE DECISION MADE: 03-AUG-22 Results: An array of matching results, dependent on which endpoint was queried.510(K) SUMMARIES OR 510(K) STATEMENTS FOR FINALĭECISIONS RENDERED DURING THE PERIOD August 2022

Meta: Metadata about the query, including a disclaimer, link to data license, last-updated date, and total matching records, if applicable. The API returns individual results as JSON by default.
#Fda 510k database how to#
Continue reading this documentation for more details on how to compose an API call for openFDA specifically.
#Fda 510k database code#
Programmatically sending the request via executing code that sends the API call and processes the response. Manually using a web browser (such as navigating to the URL ) or 2. Requests are typically sent to the API in one of two ways: 1. An API call is any request sent to the API. "API" is an acronym for Application Programming Interface. And because openFDA only serves publicly available data, it does not contain data with Personally Identifiable Information about patients or other sensitive information. Not all data in openFDA has been validated for clinical or production use.

Every query to the API must go through one endpoint for one kind of data. OpenFDA is an Elasticsearch-based API that serves public FDA data about nouns like drugs, devices, and foods.Įach of these nouns has one or more categories, which serve unique data-such as data about recall enforcement reports, or about adverse events.
