FDA Device Intelligence
Home › PRESTIGE AMERITECH, LTD. › PremierPro

PremierPro

PRESTIGE AMERITECH, LTD. · Model 2170 · UDI-DI 00818566013316

FYF
10
510(k) clearances
26
Adverse events
0
Recalls
294
Facilities

Description

PremierPro Bouffant Cap Lightweight, Pink, 21", 100/bx

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.