FDA Device Intelligence
Home › Tr Equipment AB › TR900 HI LO 230V GE

TR900 HI LO 230V GE

Tr Equipment AB · Model 05192152 · UDI-DI 07350016061377

KTC
7
510(k) clearances
101
Adverse events
0
Recalls
50
Facilities

Description

TR900 HI LO 230V GE

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.