Snap™ SNPA125US
Snap™ SNPA125US is a Class II device made by Kci USA, Inc., cleared under FDA 510(k) K112341 on 29 Aug 2011 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00849554006058), 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 | Number00849554006058 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK112341 | Date29 Aug 2011 | StatusActive |
Official records
- AccessGUDID record 00849554006058
- FDA 510(k) database K112341
Across registries
- FDA 510(k) K112341 decided 29 Aug 2011 Active
- FDA GUDID UDI-DI 00849554006058 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K112341
- Listed FDA GUDID 00849554006058
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Snap™
- Generic name
- Negative-pressure wound therapy system pump, mechanical
- Model / reference
- SNPA125US
- Primary DI / UDI-DI
- 00849554006058
- 510(k) Number
- FDA product code
- OKO
- GMDN term
- Negative-pressure wound therapy system pump, mechanical
- Device class
- Class II
- Regulation number
- 878.4683
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices
Other devices filed under FDA product code OKO (Negative Pressure Wound Therapy Non-Powered Suction Apparatus).
- CISNAP CLOSED INCISION SYSTEM by Spiracur, Inc.
- NPseal by Guard Medical, Inc.
- AnsCare SIMO NP-1-2 by BENQ MATERIALS CORP.
- SNaP Wound Care System by Spiracur, Inc.
- Anscare SIMO Negative Pressure Wound Therapy (NPWT) System by BenQ Materials Corporation
- VacHeal Negative Pressure Wound Therapy System by VacHeal, LLC
- NPseal (Small, Medium, Large) by Guard Medical, Inc.