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AutoCare E275

by Micro Current Technology, Inc.

AutoCare E275 (MF-19) is a medical device (FDA Class II; FDA product code GZJ, Stimulator, Nerve, Transcutaneous, For Pain Relief) made by Micro Current Technology, Inc., cleared under FDA 510(k) K032653 on 12 Sep 2003, registered in EUDAMED and listed in FDA GUDID since 15 Mar 2018 (UDI-DI 00817076010822), active as of 22 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K032653

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number00817076010822 UDI-DI Date15 Mar 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) GUDID from GUDID NumberK032653 Date12 Sep 2003IssuedStatusActive
European UnionCE/MDR EUDAMED Number— Date—StatusActive

Official records

Across registries

3 registries list this device

  • FDA 510(k) K032653 decided 12 Sep 2003 Active
  • EUDAMED Active
  • FDA GUDID UDI-DI 00817076010822 listed 15 Mar 2018 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K032653
  2. Listed FDA GUDID 00817076010822

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
AutoCare
Generic name
Analgesic transcutaneous electrical nerve stimulation system
Model / Ref / Catalog
E275, MF-19
Primary DI / UDI-DI
00817076010822
510(k) Number
FDA product code
GZJ
GMDN term
Analgesic transcutaneous electrical nerve stimulation system
Device class
Class II
Regulation number
882.5890
GUDID distribution status
In Commercial Distribution

Related devices

Category: Analgesic transcutaneous electrical nerve stimulation system

Similar devices

Other devices filed under FDA product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief).

Other devices from Micro Current Technology, Inc.

See all devices from Micro Current Technology, Inc. →

Properties

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