KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR— 510(k) K950358

Name: FDA 510(k) clearance K950358
Creator: U.S. Food and Drug Administration
Published: 1995-03-17

Substantially Equivalent

Storch Amini & Munves PC

FDA 510(k) clearance K950358 for KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR, Substantially Equivalent on 1995-03-17. Applicant: Storch Amini & Munves PC. Device class: 2.

Clearance details

Applicant: Storch Amini & Munves PC
Product code: Code IXW
Device class: Class 2
Regulation: 21 CFR 892.1900
Advisory panel: Radiology
Date received: 1995-01-27
Decision date: 1995-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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