KODAK DIGITAL SCIENCE FILM DIGITIZER L7501/L7506 (WITH FILM AUTOFEEDER)— 510(k) K961768
Substantially EquivalentKodak Health Imaging Systems, Inc.
FDA 510(k) clearance K961768 for KODAK DIGITAL SCIENCE FILM DIGITIZER L7501/L7506 (WITH FILM AUTOFEEDER), Substantially Equivalent on 1996-08-22. Applicant: Kodak Health Imaging Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Kodak Health Imaging Systems, Inc.
- Product code
- Code LMA
- Device class
- Class 2
- Regulation
- 21 CFR 892.2030
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dallas, TX, US
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