Nonin 9840AAT
by Nonin Medical, Inc. 2 variants
Nonin 9840AAT is a Class II device made by Nonin Medical, Inc., cleared under FDA 510(k) K982969 on 12 Aug 1999 and listed in FDA GUDID since 24 Aug 2016 (UDI-DI 00849686072068), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00849686072068 | Date24 Aug 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK982969 | Date12 Aug 1999 | StatusActive |
Official records
- AccessGUDID record 00849686072068
- FDA 510(k) database K982969
Across registries
- FDA 510(k) K982969 decided 12 Aug 1999 Active
- FDA GUDID UDI-DI 00849686072068 listed 24 Aug 2016 Listed
Timeline
- Cleared FDA 510(k) K982969
- Listed FDA GUDID 00849686072068
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Nonin
- Generic name
- Y-piece breathing circuit connector, single-use
- Model / reference
- 9840AAT
- Primary DI / UDI-DI
- 00849686072068
- 510(k) Number
- FDA product code
- CCK
- GMDN term
- Y-piece breathing circuit connector, single-use
- Device class
- Class II
- Regulation number
- 868.1400
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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