Baxter Baffled Tee Adapter
510(k) K895014
Baxter Baffled Tee Adapter is a Class I device made by Baxter Healthcare Corp, cleared under FDA 510(k) K895014 on 30 Oct 1989, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK895014 | Date30 Oct 1989 | StatusActive |
Official records
- FDA 510(k) database K895014
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- BZA
- Device class
- Class I
- Regulation
- 21 CFR Part 868.5810
- Advisory committee
- Anesthesiology
- FDA decision
- SESE Substantially Equivalent
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