Frida 02501800
Frida 02501800 is a device classified as Unclassified made by Fridababy, LLC, cleared under FDA 510(k) K220289 on 29 Jun 2022 and listed in FDA GUDID since 2 Jul 2025 (UDI-DI 00810028771697), 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 | Number00810028771697 | Date2 Jul 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK220289 | Date29 Jun 2022 | StatusActive |
Official records
- AccessGUDID record 00810028771697
- FDA 510(k) database K220289
Across registries
- FDA 510(k) K220289 decided 29 Jun 2022 Active
- FDA GUDID UDI-DI 00810028771697 listed 2 Jul 2025 Listed
Timeline
- Cleared FDA 510(k) K220289
- Listed FDA GUDID 00810028771697
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Frida
- Generic name
- Anti-nausea acupressure wristband
- Model / reference
- 02501800
- Primary DI / UDI-DI
- 00810028771697
- 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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Other devices filed under FDA product code MVV (Device, Acupressure).
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- PRESSURE RIGHT, SINGLE-USE, DISPOSABLE, PRESSURE-SENSITIVE EMETIC-MANAGEMENT WRIST STRIP by Therapeutics 101, Inc (Dba Pressure Point, Inc.)