ACQPLAN— 510(k) K974770
Substantially EquivalentPhilips Medical Systems (Cleveland), Inc.
FDA 510(k) clearance K974770 for ACQPLAN, Substantially Equivalent on 1998-09-02. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 2.
Clearance details
- Applicant
- Philips Medical Systems (Cleveland), 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
Recent devices under product code MUJ
view allMore clearances from Philips Medical Systems (Cleveland), Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.