SRX 200 DIAGNOSTIC X-RAY, HIGH VOLTAGE GENERATOR— 510(k) K850823
Substantially EquivalentPhilips Medical Systems (Cleveland), Inc.
FDA 510(k) clearance K850823 for SRX 200 DIAGNOSTIC X-RAY, HIGH VOLTAGE GENERATOR, Substantially Equivalent on 1985-04-10. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 1.
Clearance details
- Applicant
- Philips Medical Systems (Cleveland), Inc.
- Product code
- Code IZO
- Device class
- Class 1
- Regulation
- 21 CFR 892.1700
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Highland Heights, OH, US
Recent devices under product code IZO
view allMore clearances from Philips Medical Systems (Cleveland), Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.