510(k) K240996

Access Thyroglobulin Antibody II by Beckman Coulter, Inc. — Product Code JNL

K240996 is an FDA 510(k) premarket notification submitted by Beckman Coulter, Inc. for the device "Access Thyroglobulin Antibody II". The FDA issued a decision of Substantially Equivalent on July 3, 2024. The device falls under product code JNL (Immunochemical, Thyroglobulin Autoantibody), a Class II device regulated under 21 CFR 866.5870. Beckman Coulter, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 3, 2024
Date Received
April 11, 2024
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