FDA Device Intelligence
Home › AMERICAN DIAGNOSTIC CORP › Proscope™

Proscope™

AMERICAN DIAGNOSTIC CORP · Model 5215-NS · UDI-DI 00634782053536

LWF
10
510(k) clearances
217
Adverse events (2 deaths)
0
Recalls
122
Facilities

Description

Nasal Speculum,Screw Type

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.