AMETEC MASY MODULAR ANGIOSCOPE SYSTEM— 510(k) K905745

Name: FDA 510(k) clearance K905745
Creator: U.S. Food and Drug Administration
Published: 1992-04-23

Substantially Equivalent

American Medical Technology, Inc.

FDA 510(k) clearance K905745 for AMETEC MASY MODULAR ANGIOSCOPE SYSTEM, Substantially Equivalent on 1992-04-23. Applicant: American Medical Technology, Inc.. Device class: 2.

Clearance details

Applicant: American Medical Technology, Inc.
Product code: Code LYK
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1990-12-24
Decision date: 1992-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountain View, CA, US

Download summary PDF View on FDA.gov ↗

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