510(k) K911217

SR1 T4 ENZYME IMMUNOASSAY (MAGNETIC SOLID-PHASE) by Serono-Baker Diagnostics, Inc. — Product Code KLI

K911217 is an FDA 510(k) premarket notification submitted by Serono-Baker Diagnostics, Inc. for the device "SR1 T4 ENZYME IMMUNOASSAY (MAGNETIC SOLID-PHASE)". The FDA issued a decision of Substantially Equivalent on August 16, 1991. The device falls under product code KLI (Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine), a Class II device regulated under 21 CFR 862.1700. Serono-Baker Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 16, 1991
Date Received
March 19, 1991
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