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FLENTS PROTECHS

APOTHECARY PRODUCTS, LLC · Model F408-150/F408-150ST/F408-150WM1 · UDI-DI 00023185081503

EWD
10
510(k) clearances
25
Adverse events
0
Recalls
53
Facilities

Description

150 QUIET! PLEASE 10 PR 150 QP 10 PR E/P IN SHELF TRAY

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.