510(k) K922047

IGE ENZYME IMMUNOASSAY TEST KIT CAT.NO. KIF4064 by Medix Biotech, Inc. — Product Code DGC

K922047 is an FDA 510(k) premarket notification submitted by Medix Biotech, Inc. for the device "IGE ENZYME IMMUNOASSAY TEST KIT CAT.NO. KIF4064". The FDA issued a decision of Substantially Equivalent on August 5, 1992. The device falls under product code DGC (Ige, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Medix Biotech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 5, 1992
Date Received
May 1, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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