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Ambco 1000+P

by Ambco Electronics

Ambco 1000+P is a Class II device made by Ambco Electronics, listed in FDA GUDID since 12 Oct 2016 (UDI-DI 00851195007035), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00851195007035 UDI-DI Date12 Oct 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  • Withdrawn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
Ambco
Generic name
Tone audiometer, automated
Model / Ref / Catalog
1000+P
Primary DI / UDI-DI
00851195007035
FDA product code
EWO
GMDN term
Tone audiometer, automated
Device class
Class II
Regulation number
874.1050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Tone audiometer, automated

Similar devices

Other devices filed under FDA product code EWO (Audiometer).

Other devices from Ambco Electronics

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)