FDA Device Intelligence
Home › OHIO MEDICAL, LLC › Ohio

Ohio

OHIO MEDICAL, LLC · Model HS-05U2-DFXXC4 · UDI-DI 00628101528249

BYX Prescription
10
510(k) clearances
505
Adverse events (14 deaths)
1
Recalls
230
Facilities

Description

5 FT HS ASMB US N2O DF*XX 1/4'' COND

Recalls

DateFirmReason
2018-08-10A M Systems IncSome of the Disposable Smooth Interior Tubing may pull apart when stretched.

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.