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

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..

Clearance details

Applicant
Philips Medical Systems (Cleveland), Inc.
Product code
Code IYX
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Highland Heights, OH, US
Download summary PDFView on FDA.gov ↗

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