510(k) K780874

THYMUNE-T by Burroughs Wellcome Co. — Product Code DDC

K780874 is an FDA 510(k) premarket notification submitted by Burroughs Wellcome Co. for the device "THYMUNE-T". The FDA issued a decision of Substantially Equivalent on June 14, 1978. The device falls under product code DDC (Thyroglobulin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5870. Burroughs Wellcome Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 14, 1978
Date Received
May 30, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Thyroglobulin, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5870
Review Panel
IM
Submission Type