KSEA MODEL 383320 20 ANGIOMAT— 510(k) K960486

Name: FDA 510(k) clearance K960486
Creator: U.S. Food and Drug Administration
Published: 1996-10-25

Substantially Equivalent

Karl Storz Endoscopy

FDA 510(k) clearance K960486 for KSEA MODEL 383320 20 ANGIOMAT, Substantially Equivalent on 1996-10-25. Applicant: Karl Storz Endoscopy. Device class: 2.

Clearance details

Applicant: Karl Storz Endoscopy
Product code: Code DQI
Device class: Class 2
Regulation: 21 CFR 870.1800
Advisory panel: Cardiovascular
Date received: 1996-02-02
Decision date: 1996-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Culver City, CA, US

Download summary PDF View on FDA.gov ↗

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