PSW

High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Liquid

Product code
PSW
Device name
High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Liquid
Device class
Class 2
21 CFR
21 CFR 892.1570
Medical specialty
Radiology
Marketing pathway
510(K)
510(k) clearances (last 3 years)
1
Summaries archived here
1 (direct download)
510(k) clearances (all years, FDA)
7 (all years; only the last 3 years are listed here)

FDA classification definition

To provide high level disinfection of ultrasound transducers If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2023-11-21.

NumberDecision dateApplicantDevice nameSummary
K2330492023-11-21Cs Medical, LLCTD 200® Automated TEE Probe Disinfector with TD-12® …PDF

1 summaries are archived here for direct download.

Official FDA classification page: PSW
Classification and pathway per current FDA publications. Data from openFDA (CC0).