AP X-RAY TUBE ANGULATION DEVICE— 510(k) K811970

Name: FDA 510(k) clearance K811970
Creator: U.S. Food and Drug Administration
Published: 1981-08-13

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K811970 for AP X-RAY TUBE ANGULATION DEVICE, Substantially Equivalent on 1981-08-13. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 1.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code IYB
Device class: Class 1
Regulation: 21 CFR 892.1770
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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