SYNCRA TILT OPTION FOR ANGIO DIAGNOST 5— 510(k) K940696
Substantially EquivalentPhilips Medical Systems North America, Inc.
FDA 510(k) clearance K940696 for SYNCRA TILT OPTION FOR ANGIO DIAGNOST 5, Substantially Equivalent on 1994-03-16. Applicant: Philips Medical Systems North America, Inc.. Device class: 2.
Clearance details
- Applicant
- Philips Medical Systems North America, Inc.
- Product code
- Code KXJ
- Device class
- Class 2
- Regulation
- 21 CFR 892.1980
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shelton, CT, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.