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EMG Sensor 900-026

by SRS Medical Systems, Inc.

EMG Sensor 900-026 is a Class II device made by SRS Medical Systems, Inc., cleared under FDA 510(k) K063447 on 16 Aug 2007 and listed in FDA GUDID since 20 Aug 2021 (UDI-DI 00890477000180), active as of 22 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 22 Oct 2026

Documents

510(k) K063447

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00890477000180 UDI-DI Date20 Aug 2021ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK063447 Date16 Aug 2007DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K063447 decided 16 Aug 2007 Active
  • FDA GUDID UDI-DI 00890477000180 listed 20 Aug 2021 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K063447
  2. Listed FDA GUDID 00890477000180

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
EMG Sensor
Generic name
Kinesiology/electromyographic sensor set
Model / reference
900-026
Primary DI / UDI-DI
00890477000180
510(k) Number
FDA product code
HCC, IKN
GMDN term
Kinesiology/electromyographic sensor set
Device class
Class II
Regulation number
882.5050, 890.1375
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HCC (Device, Biofeedback).

Other devices from SRS Medical Systems, Inc.

See all devices from SRS Medical Systems, Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)