KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY— 510(k) K033821
Substantially EquivalentEastman Kodak Company
FDA 510(k) clearance K033821 for KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY, Substantially Equivalent on 2004-02-20. Applicant: Eastman Kodak Company. Device class: 2.
Clearance details
- Applicant
- Eastman Kodak Company
- Product code
- Code LMC
- Device class
- Class 2
- Regulation
- 21 CFR 892.2040
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Oakdale, MN, US
Recent devices under product code LMC
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