2ACHC
2ACHC is a Class II device made by Medtronic, Inc., cleared under FDA 510(k) K153139 on 6 May 2016 and listed in FDA GUDID since 23 May 2019 (UDI-DI 00763000089917), 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 | Number00763000089917 | Date23 May 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK153139 | Date6 May 2016 | StatusActive |
Official records
- AccessGUDID record 00763000089917
- FDA 510(k) database K153139
Across registries
- FDA 510(k) K153139 decided 6 May 2016 Active
- FDA GUDID UDI-DI 00763000089917 listed 23 May 2019 Listed
Timeline
- Cleared FDA 510(k) K153139
- Listed FDA GUDID 00763000089917
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Electrical-only medical device connection cable, single-use
- Model / reference
- 2ACHC
- Primary DI / UDI-DI
- 00763000089917
- 510(k) Number
- FDA product code
- DRF
- GMDN term
- Electrical-only medical device connection cable, single-use
- Device class
- Class II
- Regulation number
- 870.1220
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 1.96 Meter
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