KODAK SURECELL STREP A TEST KIT— 510(k) K881457
Substantially EquivalentEastman Kodak Company
FDA 510(k) clearance K881457 for KODAK SURECELL STREP A TEST KIT, Substantially Equivalent on 1988-04-21. Applicant: Eastman Kodak Company. Device class: 1.
Clearance details
- Applicant
- Eastman Kodak Company
- Product code
- Code GTZ
- Device class
- Class 1
- Regulation
- 21 CFR 866.3740
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rochester, NY, US
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More clearances from Eastman Kodak Company
view allData sourced from openFDA. This site is unofficial and independent of the FDA.