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High Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, Liquid

PSW · Class II — Moderate Risk (510(k) clearance required) · Radiology · 21 CFR 892.1570

Classification

FDA Product Code
PSW
Device class
Class II — Moderate Risk (510(k) clearance required)
Regulation
21 CFR 892.1570
Review panel
HO
Medical specialty
Radiology
Submission type
1
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
N

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).

Market data

Cleared 510(k) submissions
7
Registered establishments
4

Source

Authoritative
FDA Device Classification database
Machine
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