Wellcogen Group B
by Burroughs Wellcome Co. 510(k)
Active
510(k) K820069
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK820069 | Date18 Feb 1982 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 9 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- GTZ
- Device Class
- Class I
- Regulation
- 21 CFR Part 866.3740
- Advisory Committee
- Microbiology
- FDA Decision
- SESE Substantially Equivalent