510(k) K924119

VENTREX ALLERGEN DISC by Ventrex, Inc. — Product Code DHB

K924119 is an FDA 510(k) premarket notification submitted by Ventrex, Inc. for the device "VENTREX ALLERGEN DISC". The FDA issued a decision of Substantially Equivalent on November 30, 1992. The device falls under product code DHB (System, Test, Radioallergosorbent (Rast) Immunological), a Class II device regulated under 21 CFR 866.5750. Ventrex, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 30, 1992
Date Received
August 14, 1992
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