CX250 MOBILE GAMMA CAMERA & DCS CONSOLE— 510(k) K880878
Substantially EquivalentPhilips 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
Data sourced from openFDA. This site is unofficial and independent of the FDA.