510(k) K892853

T4 CLASP-BEAD EIA KIT by Biotecx Laboratories, Inc. — Product Code KLI

K892853 is an FDA 510(k) premarket notification submitted by Biotecx Laboratories, Inc. for the device "T4 CLASP-BEAD EIA KIT". The FDA issued a decision of Substantially Equivalent on May 22, 1989. The device falls under product code KLI (Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine), a Class II device regulated under 21 CFR 862.1700. Biotecx Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 22, 1989
Date Received
April 18, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine
Device Class
Class II
Regulation Number
862.1700
Review Panel
CH
Submission Type