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ClearScan™ A10004-5

by Graphic Controls Acquisition Corp

ClearScan™ A10004-5 is a Class II device made by Graphic Controls Acquisition Corp, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 10813150020142), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10813150020142 UDI-DI Date16 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
ClearScan™
Generic name
Electrocardiographic electrode, single-use
Model / Ref / Catalog
A10004-5
Primary DI / UDI-DI
10813150020142
FDA product code
DRX
GMDN term
Electrocardiographic electrode, single-use
Device class
Class II
Regulation number
870.2360
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Electrocardiographic electrode, single-use

Similar devices in this category

Other devices filed under Electrocardiographic electrode, single-use.

Other devices from Graphic Controls Acquisition Corp

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Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)