510(k) K891068

VENTREX COATED TUBE T3 UPTAKE by Ventrex Laboratories, Inc. — Product Code KHQ

K891068 is an FDA 510(k) premarket notification submitted by Ventrex Laboratories, Inc. for the device "VENTREX COATED TUBE T3 UPTAKE". The FDA issued a decision of Substantially Equivalent on April 10, 1989. The device falls under product code KHQ (Radioassay, Triiodothyronine Uptake), a Class II device regulated under 21 CFR 862.1715. Ventrex Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 10, 1989
Date Received
March 1, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioassay, Triiodothyronine Uptake
Device Class
Class II
Regulation Number
862.1715
Review Panel
CH
Submission Type