510(k) K780874
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