510(k) K864512

IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/HUMAN HAPTO by Cooper Biomedical, Inc. — Product Code DAD

K864512 is an FDA 510(k) premarket notification submitted by Cooper Biomedical, Inc. for the device "IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/HUMAN HAPTO". The FDA issued a decision of Substantially Equivalent on February 13, 1987. The device falls under product code DAD (Haptoglobin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5460. Cooper Biomedical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 13, 1987
Date Received
November 13, 1986
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