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.
Clearance details
- Applicant
- Eastman Kodak Company
- Product code
- Code LMC
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Oakdale, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.