BIO SCAN-BG(TM— 510(k) K910692

Substantially Equivalent

Bio Scan Instrument, Inc.

FDA 510(k) clearance K910692 for BIO SCAN-BG(TM, Substantially Equivalent on 1991-03-29. Applicant: Bio Scan Instrument, Inc..

Clearance details

Applicant: Bio Scan Instrument, Inc.
Product code: Code CGA
Advisory panel: Clinical Chemistry
Date received: 1991-02-19
Decision date: 1991-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

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Adverse events under product code CGA

product code CGA

Death: 2
Malfunction: 1,816
Total: 1,818

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.