ANGIOSCOPE— 510(k) K894459

Substantially Equivalent

Intramed Laboratories, Inc.

FDA 510(k) clearance K894459 for ANGIOSCOPE, Substantially Equivalent on 1990-03-07. Applicant: Intramed Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Intramed Laboratories, Inc.
Product code: Code LYK
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1989-07-18
Decision date: 1990-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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