FDA Device Intelligence
Home › O&M HALYARD, INC. › Halyard

Halyard

O&M HALYARD, INC. · Model 69520 · UDI-DI 20680651695202

FYF
10
510(k) clearances
28
Adverse events
0
Recalls
294
Facilities

Description

HALYARD* Surgical Cap-3-Layer SMS on Sides, Spunbond on Top

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.