FDA Device Intelligence
HomeINSTRUMENTATION LABORATORY COMPANY › HemosIL Factor XIII Antigen

HemosIL Factor XIII Antigen

INSTRUMENTATION LABORATORY COMPANY · Model 00020201300 · UDI-DI 08426950358725

DBT Prescription
1
510(k) clearances
1
Adverse events
0
Recalls
6
Facilities

Description

HemosIL Factor XIII Antigen

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data 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.