UHE COLLIMATOR (210591)— 510(k) K963406

Name: FDA 510(k) clearance K963406
Creator: U.S. Food and Drug Administration
Published: 1997-02-26

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K963406 for UHE COLLIMATOR (210591), Substantially Equivalent on 1997-02-26. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 2.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code KPS
Device class: Class 2
Regulation: 21 CFR 892.1200
Advisory panel: Radiology
Date received: 1996-08-29
Decision date: 1997-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cleveland, OH, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.