MED2000 Nebulizer Compressor, Models P3, P4, P5 with Nebulizer
by Med2000 S.R.L. 510(k)
Active
510(k) K041974
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK041974 | Date24 Aug 2004 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- BTI
- Models / Variants
- Device Class
- Class II
- Regulation
- 21 CFR Part 868.6250
- Advisory Committee
- Anesthesiology
- FDA Decision
- SESE Substantially Equivalent