Empty Viaflex Plastic Container
510(k) K922214
Empty Viaflex Plastic Container is a Class II device made by Baxter Healthcare Corp, cleared under FDA 510(k) K922214 on 26 Mar 1993, 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 | NumberK922214 | Date26 Mar 1993 | StatusActive |
Official records
- FDA 510(k) database K922214
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KPE
- Device class
- Class II
- Regulation
- 21 CFR Part 880.5025
- Advisory committee
- General Hospital
- FDA decision
- SESE Substantially Equivalent
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