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Grip Strength Device (Gsd)

by Devcom, Inc. 510(k)

Active United States

510(k) K863313

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK863313 Date9 Sep 1986ClearedStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
IKK
Device Class
Class II
Regulation
21 CFR Part 890.1925
Advisory Committee
Physical Medicine
FDA Decision
SESE Substantially Equivalent

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