510(k) K864142

UBI MAGIWEL(TM) IGE QUANTITATIVE AND QUALITATIVE by United Biotech, Inc. — Product Code DGC

K864142 is an FDA 510(k) premarket notification submitted by United Biotech, Inc. for the device "UBI MAGIWEL(TM) IGE QUANTITATIVE AND QUALITATIVE". The FDA issued a decision of Substantially Equivalent on December 3, 1986. The device falls under product code DGC (Ige, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. United Biotech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 3, 1986
Date Received
October 22, 1986
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