Unimed MAS-LNCS Pdtx
by Unimed Medical Supplies, Inc.
Unimed MAS-LNCS Pdtx is a Class II device made by Unimed Medical Supplies, Inc., cleared under FDA 510(k) K142832 on 6 Feb 2015 and listed in FDA GUDID since 16 Mar 2020 (UDI-DI 06945664876346), 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 | GUDID listing | Number06945664876346 | Date16 Mar 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK142832 | Date6 Feb 2015 | StatusActive |
Official records
- AccessGUDID record 06945664876346
- FDA 510(k) database K142832
Across registries
- FDA 510(k) K142832 decided 6 Feb 2015 Active
- FDA GUDID UDI-DI 06945664876346 listed 16 Mar 2020 Listed
Timeline
- Cleared FDA 510(k) K142832
- Listed FDA GUDID 06945664876346
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Unimed
- Generic name
- Pulse oximeter probe, single-use
- Model / reference
- MAS-LNCS Pdtx
- Primary DI / UDI-DI
- 06945664876346
- 510(k) Number
- FDA product code
- DQA
- GMDN term
- Pulse oximeter probe, single-use
- Device class
- Class II
- Regulation number
- 870.2700
- GUDID distribution status
- In Commercial Distribution
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