MODIFICATION TO KODAK DIRECTVIEW CR 800/900 SYSTEM— 510(k) K021829
Substantially EquivalentEastman Kodak Company
FDA 510(k) clearance K021829 for MODIFICATION TO KODAK DIRECTVIEW CR 800/900 SYSTEM, Substantially Equivalent on 2002-07-02. Applicant: Eastman Kodak Company. Device class: 2.
Clearance details
- Applicant
- Eastman Kodak Company
- Product code
- Code MQB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Rochester, NY, US
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