Emergency Relief Kit System
510(k) K964029
Emergency Relief Kit System is a device classified as Not classified made by Baxter Healthcare Corp, cleared under FDA 510(k) K964029 on 17 Mar 1997, 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)SEKD | NumberK964029 | Date17 Mar 1997 | StatusActive |
Official records
- FDA 510(k) database K964029
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LRR
- Device class
- N
- Advisory committee
- Unknown
- FDA decision
- SEKD
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