HUMAN C1Q RADIAL IMMUNODIFFUSION KIT— 510(k) K951968

Substantially Equivalent

Kent Laboratories, Inc.

FDA 510(k) clearance K951968 for HUMAN C1Q RADIAL IMMUNODIFFUSION KIT, Substantially Equivalent on 1995-05-30. Applicant: Kent Laboratories, Inc..

Clearance details

Applicant: Kent Laboratories, Inc.
Product code: Code DAK
Advisory panel: Immunology
Date received: 1995-04-27
Decision date: 1995-05-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redmond, WA, US

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