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Polysonic Ultrasound Lotion

by Parker Laboratories, Inc.

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.

Overview

A comprehensive review of the Polysonic Ultrasound Lotion, including its features, compliance, and FAQs.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00855683006319 UDI-DI Date19 Dec 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  • Withdrawn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
Polysonic
Generic name
Electrode conductive medium
Model / Ref / Catalog
ULTRASOUND LOTION, 21-28
Primary DI / UDI-DI
00855683006319
FDA product code
IYO
GMDN term
Electrode conductive medium
Device class
Class II
Regulation number
892.1560
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IYO (System, Imaging, Pulsed Echo, Ultrasonic).

Other devices from Parker Laboratories, Inc.

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Properties

  • Single use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)