CX250 MOBILE GAMMA CAMERA & DCS CONSOLE— 510(k) K880878

Name: FDA 510(k) clearance K880878
Creator: U.S. Food and Drug Administration
Published: 1988-09-01

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K880878 for CX250 MOBILE GAMMA CAMERA & DCS CONSOLE, Substantially Equivalent on 1988-09-01. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 1.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code IYX
Device class: Class 1
Regulation: 21 CFR 892.1100
Advisory panel: Radiology
Date received: 1988-03-01
Decision date: 1988-09-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Highland Heights, OH, US

Download summary PDF View on FDA.gov ↗

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