Polysonic Ultrasound Lotion
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Overview
A comprehensive review of the Polysonic Ultrasound Lotion, including its features, compliance, and FAQs.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00855683006319 | Date19 Dec 2016 | StatusListed |
Official records
- AccessGUDID record 00855683006319
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- 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).
- Minivisor Terminal by Organon Teknika Corp.
- bk3000, bk3500, bk5000, bkActiv 2300 by Bk Medical ApS
- Sound Imager I by Sound Imaging, Inc.
- B-scan Plus- VET 24-6100-V by ACCUTOME, INC.
- Echo. Akho by Alliance Medical, Inc.
- BladderScan Prime System by Verathon Incorporated
- Sonoace 5500 Diagnostic Ultrasound System by Medison America, Inc.
- Volcano IFR Modality by VOLCANO CORPORATION
- System, Echo, Pulsed Ultrasonic Diag by General Electric Co.
- 5.0 Mhz Array Intravaginal Transducer by Advanced Technology Laboratories, Inc.