RADIAL IMMUNO-TEST FOR HUMAN C-REACTI— 510(k) K831958
Substantially EquivalentKent Laboratories, Inc.
FDA 510(k) clearance K831958 for RADIAL IMMUNO-TEST FOR HUMAN C-REACTI, Substantially Equivalent on 1983-07-19. Applicant: Kent Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Kent Laboratories, Inc.
- Product code
- Code DCK
- Device class
- Class 2
- Regulation
- 21 CFR 866.5270
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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