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Somatosensory Stimulus System

by Biomagnetic Technologies, Inc.

510(k) K913604

Somatosensory Stimulus System is a Class II device made by Biomagnetic Technologies, Inc., cleared under FDA 510(k) K913604 on 9 Dec 1991, active as of 22 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 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK913604 Date9 Dec 1991ClearedStatusActive

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  • Withdrawn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
GZP
Device class
Class II
Regulation
21 CFR Part 882.1880
Advisory committee
Neurology
FDA decision
SESE Substantially Equivalent

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