FDA Device Intelligence
Home › INSTRUMENTATION LABORATORY COMPANY › HemosIL FII & FV DNA Control

HemosIL FII & FV DNA Control

INSTRUMENTATION LABORATORY COMPANY · Model 00020003500 · UDI-DI 08426950453086

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

Description

HemosIL FII & FV DNA Control

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.