HUMAN LYME EIA FOR THE DETECT OF ANTIBODIES— 510(k) K890281
Substantially EquivalentCambridge Bioscience Corp.
FDA 510(k) clearance K890281 for HUMAN LYME EIA FOR THE DETECT OF ANTIBODIES, Substantially Equivalent on 1989-03-15. Applicant: Cambridge Bioscience Corp.. Device class: 2.
Clearance details
- Applicant
- Cambridge Bioscience Corp.
- Product code
- Code LSR
- Device class
- Class 2
- Regulation
- 21 CFR 866.3830
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Worcester, MA, US
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