510(k) K233049

TD 200® Automated TEE Probe Disinfector with TD-12® High-Level Disinfectant with QwikCheck™ Chemical Indicator by Cs Medical, LLC — Product Code PSW

K233049 is an FDA 510(k) premarket notification submitted by Cs Medical, LLC for the device "TD 200® Automated TEE Probe Disinfector with TD-12® High-Level Disinfectant with QwikCheck™ Chemical Indicator". The FDA issued a decision of Substantially Equivalent on November 21, 2023. The device falls under product code PSW (High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Liquid), a Class II device regulated under 21 CFR 892.1570. Cs Medical, LLC has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 21, 2023
Date Received
September 25, 2023
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Liquid
Device Class
Class II
Regulation Number
892.1570
Review Panel
HO
Submission Type

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).