FDA Device Intelligence
HomeCIVCO MEDICAL INSTRUMENTS CO., INC. › GUS

GUS

CIVCO MEDICAL INSTRUMENTS CO., INC. · Model 610-921 · UDI-DI 00841436112352

PHT
0
510(k) clearances
1
Adverse events
0
Recalls
15
Facilities

Description

G10VPL Gus system

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.