Amc Cb-2462263
Amc Cb-2462263 is a Class II device made by LifeSync Corporation, cleared under FDA 510(k) K992524 on 1 Mar 2000 and listed in FDA GUDID since 23 Apr 2018 (UDI-DI 00849593010245), 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 | Number00849593010245 | Date23 Apr 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK992524 | Date1 Mar 2000 | StatusActive |
Official records
- AccessGUDID record 00849593010245
- FDA 510(k) database K992524
Across registries
- FDA 510(k) K992524 decided 1 Mar 2000 Active
- FDA GUDID UDI-DI 00849593010245 listed 23 Apr 2018 Listed
Timeline
- Cleared FDA 510(k) K992524
- Listed FDA GUDID 00849593010245
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Amc
- Generic name
- Electrical-only medical device connection cable, reusable
- Model / reference
- CB-2462263
- Primary DI / UDI-DI
- 00849593010245
- 510(k) Number
- FDA product code
- DSA
- GMDN term
- Electrical-only medical device connection cable, reusable
- Device class
- Class II
- Regulation number
- 870.2900
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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