FDA Device Intelligence
Home › BIO-RAD LABORATORIES, INC. › VARIANT II

VARIANT II

BIO-RAD LABORATORIES, INC. · Model 2702000 · UDI-DI 00847817014949

LDM
10
510(k) clearances
7
Adverse events
1
Recalls
10
Facilities

Description

VARIANT II

Recalls

DateFirmReason
2003-11-17Abbott Health Products, Inc.Drug product cross reacts with the Tricyclic Antidepressants (TCA) assay.

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.