Infant Evaluation Carrier
by E.M. Adams
510(k) K831731
Infant Evaluation Carrier is a Class I device made by E.M. Adams, cleared under FDA 510(k) K831731 on 18 Jul 1983, 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 | NumberK831731 | Date18 Jul 1983 | StatusActive |
Official records
- FDA 510(k) database K831731
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- FPP
- Device class
- Class I
- Regulation
- 21 CFR Part 880.6900
- Advisory committee
- General Hospital
- FDA decision
- SESE Substantially Equivalent
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