510(k) K822472

ANTISERA TO HUMAN FERRITIN by Kent Laboratories, Inc. — Product Code DBF

K822472 is an FDA 510(k) premarket notification submitted by Kent Laboratories, Inc. for the device "ANTISERA TO HUMAN FERRITIN". The FDA issued a decision of Substantially Equivalent on September 30, 1982. The device falls under product code DBF (Ferritin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5340. Kent Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 30, 1982
Date Received
August 17, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ferritin, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5340
Review Panel
IM
Submission Type