510(k) K831957

DETERM. SIZE 72 RADIAL HUMAN HAPTOGLOB by Kent Laboratories, Inc. — Product Code DAD

K831957 is an FDA 510(k) premarket notification submitted by Kent Laboratories, Inc. for the device "DETERM. SIZE 72 RADIAL HUMAN HAPTOGLOB". The FDA issued a decision of Substantially Equivalent on July 18, 1983. The device falls under product code DAD (Haptoglobin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5460. Kent Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 18, 1983
Date Received
June 17, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Haptoglobin, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5460
Review Panel
IM
Submission Type