510(k) K852999

QVANTIMETRIC 2KAPPA AND LAMBDA TEST KIT by Kallestad Laboratories, Inc. — Product Code DEH

K852999 is an FDA 510(k) premarket notification submitted by Kallestad Laboratories, Inc. for the device "QVANTIMETRIC 2KAPPA AND LAMBDA TEST KIT". The FDA issued a decision of Substantially Equivalent on October 21, 1985. The device falls under product code DEH (Lambda, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5550. Kallestad Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 21, 1985
Date Received
July 15, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Lambda, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5550
Review Panel
IM
Submission Type