510(k) K905636

VENTREX COATED TUBE IGE ENZYME IMMUNOASSAY by Ventrex Laboratories, Inc. — Product Code DHB

K905636 is an FDA 510(k) premarket notification submitted by Ventrex Laboratories, Inc. for the device "VENTREX COATED TUBE IGE ENZYME IMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on February 7, 1991. The device falls under product code DHB (System, Test, Radioallergosorbent (Rast) Immunological), a Class II device regulated under 21 CFR 866.5750. Ventrex Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 7, 1991
Date Received
December 17, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Radioallergosorbent (Rast) Immunological
Device Class
Class II
Regulation Number
866.5750
Review Panel
IM
Submission Type