510(k) K792484

TIPSEP-T3U TRIIODOTHYRONINE UPTAKE by Nuclear Diagnostics, Inc. — Product Code KHQ

K792484 is an FDA 510(k) premarket notification submitted by Nuclear Diagnostics, Inc. for the device "TIPSEP-T3U TRIIODOTHYRONINE UPTAKE". The FDA issued a decision of Substantially Equivalent on December 27, 1979. The device falls under product code KHQ (Radioassay, Triiodothyronine Uptake), a Class II device regulated under 21 CFR 862.1715. Nuclear Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 27, 1979
Date Received
December 3, 1979
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