510(k) K895186

FIAGEN T3 UPTAKE CATALOGUE #101-402 by Cyberfluor, Inc. — Product Code KHQ

K895186 is an FDA 510(k) premarket notification submitted by Cyberfluor, Inc. for the device "FIAGEN T3 UPTAKE CATALOGUE #101-402". The FDA issued a decision of Substantially Equivalent on November 8, 1989. The device falls under product code KHQ (Radioassay, Triiodothyronine Uptake), a Class II device regulated under 21 CFR 862.1715. Cyberfluor, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 8, 1989
Date Received
August 11, 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