510(k) K192228

CS Medical TD 200 disinfector with TD-12 high-level disinfectant, CS Medical TD-12 high-level disinfectant by Cs Medical, LLC — Product Code PSW

K192228 is an FDA 510(k) premarket notification submitted by Cs Medical, LLC for the device "CS Medical TD 200 disinfector with TD-12 high-level disinfectant, CS Medical TD-12 high-level disinfectant". The FDA issued a decision of Substantially Equivalent on April 1, 2020. 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
April 1, 2020
Date Received
August 16, 2019
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).