SLIDEX STAPH-KIT— 510(k) K923212
Substantially EquivalentBiomerieux Vitek, Inc.
FDA 510(k) clearance K923212 for SLIDEX STAPH-KIT, Substantially Equivalent on 1992-09-28. Applicant: Biomerieux Vitek, Inc.. Device class: 1.
Clearance details
- Applicant
- Biomerieux Vitek, Inc.
- Product code
- Code JWX
- Device class
- Class 1
- Regulation
- 21 CFR 866.2660
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hazelwood, MO, US
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