MyoPad Vault PB-250
MyoPad Vault PB-250 is a Class I device made by Precision Biometrics Inc, cleared under FDA 510(k) K123399 on 1 Aug 2013 and listed in FDA GUDID since 13 Dec 2016 (UDI-DI 00853818007279), 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 | Number00853818007279 | Date13 Dec 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK123399 | Date1 Aug 2013 | StatusActive |
Official records
- AccessGUDID record 00853818007279
- FDA 510(k) database K123399
Across registries
- FDA 510(k) K123399 decided 1 Aug 2013 Active
- FDA GUDID UDI-DI 00853818007279 listed 13 Dec 2016 Listed
Timeline
- Cleared FDA 510(k) K123399
- Listed FDA GUDID 00853818007279
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MyoPad Vault
- Generic name
- Electrode conductive medium
- Model / reference
- PB-250
- Primary DI / UDI-DI
- 00853818007279
- 510(k) Number
- FDA product code
- KQX, HCS, HCC, IKN
- GMDN term
- Electrode conductive medium
- Device class
- Class I
- Regulation number
- 888.1500, 882.1570, 882.5050, 890.1375
- GUDID distribution status
- In Commercial Distribution
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