CLINIX-R TOMOGRAPHIC DEVICE— 510(k) K810274

Name: FDA 510(k) clearance K810274
Creator: U.S. Food and Drug Administration
Published: 1981-03-11

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K810274 for CLINIX-R TOMOGRAPHIC DEVICE, Substantially Equivalent on 1981-03-11. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 2.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code IZF
Device class: Class 2
Regulation: 21 CFR 892.1740
Advisory panel: Radiology
Date received: 1981-02-02
Decision date: 1981-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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