AP X-RAY TUBE ANGULATION DEVICE— 510(k) K811970
Substantially EquivalentPhilips Medical Systems (Cleveland), Inc.
FDA 510(k) clearance K811970 for AP X-RAY TUBE ANGULATION DEVICE, Substantially Equivalent on 1981-08-13. Applicant: Philips Medical Systems (Cleveland), Inc..
Clearance details
- Applicant
- Philips Medical Systems (Cleveland), Inc.
- Product code
- Code IYB
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.