510(k) K791285

ANTI-HUMAN GLOBULINS by Diagnostica, Inc. — Product Code DEW

K791285 is an FDA 510(k) premarket notification submitted by Diagnostica, Inc. for the device "ANTI-HUMAN GLOBULINS". The FDA issued a decision of Substantially Equivalent on October 17, 1979. The device falls under product code DEW (Igg, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Diagnostica, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 17, 1979
Date Received
July 10, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Igg, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5510
Review Panel
IM
Submission Type