The Electrode Store 62056
by Impulse Medical Technologies, Inc.
The Electrode Store 62056 is a Class II device made by Impulse Medical Technologies, Inc., cleared under FDA 510(k) K020910 on 19 Jul 2002 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00816022022087), 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 | Number00816022022087 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK020910 | Date19 Jul 2002 | StatusActive |
Official records
- AccessGUDID record 00816022022087
- FDA 510(k) database K020910
Across registries
- FDA 510(k) K020910 decided 19 Jul 2002 Active
- FDA GUDID UDI-DI 00816022022087 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K020910
- Listed FDA GUDID 00816022022087
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- The Electrode Store
- Generic name
- Subdermal needle electrode
- Model / Ref / Catalog
- 62056
- Primary DI / UDI-DI
- 00816022022087
- 510(k) Number
- FDA product code
- GXZ
- GMDN term
- Subdermal needle electrode
- Device class
- Class II
- Regulation number
- 882.1350
- GUDID distribution status
- In Commercial Distribution