510(k) K905612

VENTREX COATED TUBE IGE RADIOIMMUNOASSAY by Ventrex Laboratories, Inc. — Product Code DGC

K905612 is an FDA 510(k) premarket notification submitted by Ventrex Laboratories, Inc. for the device "VENTREX COATED TUBE IGE RADIOIMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on February 21, 1991. The device falls under product code DGC (Ige, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Ventrex Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 21, 1991
Date Received
December 14, 1990
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