KODAK LANEX MED. SCREEN— 510(k) K792123
Substantially EquivalentEastman Kodak Company
FDA 510(k) clearance K792123 for KODAK LANEX MED. SCREEN, Substantially Equivalent on 1979-12-10. Applicant: Eastman Kodak Company. Device class: 1.
Clearance details
- Applicant
- Eastman Kodak Company
- Product code
- Code EAM
- Device class
- Class 1
- Regulation
- 21 CFR 892.1960
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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