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CAT Pro Select CT012

by J-Tech Medical, Inc.

CAT Pro Select CT012 is a joint/spinal manipulator (FDA unclassified; FDA product code LXM, Manipulator, Plunger-Like Joint) made by J-Tech Medical, Inc., cleared under FDA 510(k) K974376 on 18 Feb 1998 and listed in FDA GUDID since 14 May 2021 (UDI-DI G041CT0120), 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) K974376

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 NumberG041CT0120 UDI-DI Date14 May 2021ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK974376 Date18 Feb 1998DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K974376 decided 18 Feb 1998 Active
  • FDA GUDID UDI-DI G041CT0120 listed 14 May 2021 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K974376
  2. Listed FDA GUDID G041CT0120

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
CAT Pro Select
Generic name
Joint/spinal manipulator, mechanical
Model / reference
CT012
Primary DI / UDI-DI
G041CT0120
510(k) Number
FDA product code
LXM
GMDN term
Joint/spinal manipulator, mechanical
Device class
U
GUDID distribution status
In Commercial Distribution

Related devices

Category: Joint/spinal manipulator, mechanical

Cleared under the same submission (K974376)

Similar devices

Other devices filed under FDA product code LXM (Manipulator, Plunger-Like Joint).

Other devices from J-Tech Medical, Inc.

See all devices from J-Tech Medical, Inc. →

Properties

Other properties (15, all answered No)