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Amc Cb-2462263

by LifeSync Corporation

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 United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K992524

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00849593010245 UDI-DI Date23 Apr 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK992524 Date1 Mar 2000DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K992524 decided 1 Mar 2000 Active
  • FDA GUDID UDI-DI 00849593010245 listed 23 Apr 2018 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K992524
  2. Listed FDA GUDID 00849593010245

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

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

Similar devices in this category

Other devices filed under Electrical-only medical device connection cable, reusable.

Other devices from LifeSync Corporation

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Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)