510(k) K843672

Q-FEVER by Institute Virion , Ltd. — Product Code GPS

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 8, 1985
Date Received
September 17, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antigen, Cf, Q Fever
Device Class
Class I
Regulation Number
866.3500
Review Panel
MI
Submission Type