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Scantibodies Laboratory, Inc.
SCANTIBODIES LABORATORY, INC. · Model 3KG556 · UDI-DI 00850002253153
10
510(k) clearances
38
Adverse events
1
Recalls
11
Facilities
Description
Calcitonin IRMA (Coated Tube)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-09-18 | Biomerica | A potential issue with false high values. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.