MICRO-ELISA TSH TEST KIT-VISI-CHECK TSH TEST KIT— 510(k) K854379

Substantially Equivalent

Bioclinical Systems, Inc.

FDA 510(k) clearance K854379 for MICRO-ELISA TSH TEST KIT-VISI-CHECK TSH TEST KIT, Substantially Equivalent on 1986-01-07. Applicant: Bioclinical Systems, Inc..

Clearance details

Applicant: Bioclinical Systems, Inc.
Product code: Code JLW
Advisory panel: Clinical Chemistry
Date received: 1985-10-30
Decision date: 1986-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St.Louis, MO, US

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Adverse events under product code JLW

product code JLW

Malfunction: 885
Total: 885

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.