KARL STORZ TWIN TRANSILLUMINATOR— 510(k) K962032

Name: FDA 510(k) clearance K962032
Creator: U.S. Food and Drug Administration
Published: 1996-07-05

Substantially Equivalent

KARL STORZ Endoscopy-America, Inc.

FDA 510(k) clearance K962032 for KARL STORZ TWIN TRANSILLUMINATOR, Substantially Equivalent on 1996-07-05. Applicant: KARL STORZ Endoscopy-America, Inc.. Device class: 1.

Clearance details

Applicant: KARL STORZ Endoscopy-America, Inc.
Product code: Code MQW
Device class: Class 1
Regulation: 21 CFR 874.4350
Advisory panel: Ear, Nose, Throat
Date received: 1996-05-24
Decision date: 1996-07-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Culver City, CA, US

Download summary PDF View on FDA.gov ↗

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