GE ADVANTAGE DIGITIZER WORKSTATION— 510(k) K970628
Substantially EquivalentGe Medical Systems, Inc.
FDA 510(k) clearance K970628 for GE ADVANTAGE DIGITIZER WORKSTATION, Substantially Equivalent on 1997-05-12. Applicant: Ge Medical Systems, Inc.. Device class: 1.
Clearance details
- Applicant
- Ge Medical Systems, Inc.
- Product code
- Code LMD
- Device class
- Class 1
- Regulation
- 21 CFR 892.2020
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Milwaukee, WI, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.