READAR— 510(k) K930478
Substantially EquivalentAlamar Biosciences, Inc.
FDA 510(k) clearance K930478 for READAR, Substantially Equivalent on 1993-10-22. Applicant: Alamar Biosciences, Inc.. Device class: 2.
Clearance details
- Applicant
- Alamar Biosciences, Inc.
- Product code
- Code LRG
- Device class
- Class 2
- Regulation
- 21 CFR 866.1640
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Sacramento, CA, US
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