CP-625 SEE-THRU FILM CHANGER— 510(k) K811967

Name: FDA 510(k) clearance K811967
Creator: U.S. Food and Drug Administration
Published: 1981-08-13

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K811967 for CP-625 SEE-THRU FILM CHANGER, Substantially Equivalent on 1981-08-13. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 2.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code KPX
Device class: Class 2
Regulation: 21 CFR 892.1860
Advisory panel: Radiology
Date received: 1981-07-10
Decision date: 1981-08-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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