510(k) K880547

VENTREZYME VAST IMMUNO-PEROXIDASE ASSAY by Ventrex Laboratories, Inc. — Product Code DHB

K880547 is an FDA 510(k) premarket notification submitted by Ventrex Laboratories, Inc. for the device "VENTREZYME VAST IMMUNO-PEROXIDASE ASSAY". The FDA issued a decision of Substantially Equivalent on March 25, 1988. 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
March 25, 1988
Date Received
February 9, 1988
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