MumEase AB1
by Mumease
MumEase AB1 is a device classified as Unclassified made by Mumease, cleared under FDA 510(k) K193374 on 4 Mar 2020 and listed in FDA GUDID since 9 Apr 2020 (UDI-DI 00860000032803), 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 | Number00860000032803 | Date9 Apr 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK193374 | Date4 Mar 2020 | StatusActive |
Official records
- AccessGUDID record 00860000032803
- FDA 510(k) database K193374
Across registries
- FDA 510(k) K193374 decided 4 Mar 2020 Active
- FDA GUDID UDI-DI 00860000032803 listed 9 Apr 2020 Listed
Timeline
- Cleared FDA 510(k) K193374
- Listed FDA GUDID 00860000032803
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MumEase
- Generic name
- Anti-nausea acupressure wristband
- Model / reference
- AB1
- Primary DI / UDI-DI
- 00860000032803
- 510(k) Number
- FDA product code
- MVV
- GMDN term
- Anti-nausea acupressure wristband
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
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