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None Dsphgelp-10

by Neurovision Medical Products Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB006HGELP102 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
None
Generic Name
Analytical non-scalp cutaneous electrode
Model / Ref / Catalog
DSPHGELP-10
Primary DI / UDI-DI
B006HGELP102
510(k) Number
FDA Product Code
ETN
GMDN Term
Analytical non-scalp cutaneous electrode
Device Class
Class II
Regulation Number
874.1820
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Analytical non-scalp cutaneous electrode

Cleared under the same submission (K110138)

Other devices from Neurovision Medical Products Inc.

See all devices from Neurovision Medical Products Inc. →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No