MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA— 510(k) K904050
Substantially EquivalentPhilips Medical Systems (Cleveland), Inc.
FDA 510(k) clearance K904050 for MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA, Substantially Equivalent on 1990-12-05. 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
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cleveland, OH, US
Recent devices under product code IYX
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