EZ-SCREEN:HCG— 510(k) K902681

Substantially Equivalent

Environmental Diagnostics, Inc.

FDA 510(k) clearance K902681 for EZ-SCREEN:HCG, Substantially Equivalent on 1990-08-09. Applicant: Environmental Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant
Environmental Diagnostics, Inc.
Product code
Code JHI
Device class
Class 2
Regulation
21 CFR 862.1155
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Burlington, NC, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code JHI

product code JHI
Malfunction
1,055
Total
1,055

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.