ACQPLAN 5.0— 510(k) K013644
Substantially EquivalentPhilips Medical Systems, Inc.
FDA 510(k) clearance K013644 for ACQPLAN 5.0, Substantially Equivalent on 2002-09-12. Applicant: Philips Medical Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Philips Medical Systems, Inc.
- Product code
- Code MUJ
- Device class
- Class 2
- Regulation
- 21 CFR 892.5050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cleveland, OH, US
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