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Med-Tec Hand Grip

by Medtec LLC

510(k) K954225

Med-Tec Hand Grip is a Class II device made by Medtec LLC, cleared under FDA 510(k) K954225 on 14 Nov 1995, active as of 10 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 10 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 10 Oct 2026.

Regulatory status

as of registry sync 10 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK954225 Date14 Nov 1995ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
IXQ
FDA applicant
Medtec, Inc.
Device class
Class II
Regulation
21 CFR Part 892.1980
Advisory committee
Radiology
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code IXQ (Table, Radiographic, Stationary Top).

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