510(k) K811828

SICKLE CELL REAGENT SET by Anco Medical Reagents & Assoc. — Product Code GHM

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 12, 1981
Date Received
June 29, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Test, Sickle Cell
Device Class
Class II
Regulation Number
864.7825
Review Panel
HE
Submission Type