KODAK MEDICAL X-RAY DEVELOPER & REPLEN.— 510(k) K801209
Substantially EquivalentEastman Kodak Company
FDA 510(k) clearance K801209 for KODAK MEDICAL X-RAY DEVELOPER & REPLEN., Substantially Equivalent on 1980-06-26. Applicant: Eastman Kodak Company.
Clearance details
- Applicant
- Eastman Kodak Company
- Product code
- Code IXW
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.