510(k) K951362

THYROGLOBULIN EIA TEST KIT by Immunoprobe, Inc. — Product Code JNL

K951362 is an FDA 510(k) premarket notification submitted by Immunoprobe, Inc. for the device "THYROGLOBULIN EIA TEST KIT". The FDA issued a decision of Substantially Equivalent on November 20, 1995. The device falls under product code JNL (Immunochemical, Thyroglobulin Autoantibody), a Class II device regulated under 21 CFR 866.5870. Immunoprobe, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 20, 1995
Date Received
March 24, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Immunochemical, Thyroglobulin Autoantibody
Device Class
Class II
Regulation Number
866.5870
Review Panel
IM
Submission Type