Custom Ultrasonics, Inc.
Custom Ultrasonics, Inc. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2020, with 2 FDA device recalls on record.
Top product codes for Custom Ultrasonics, Inc.
FDA recalls by Custom Ultrasonics, Inc.
- Z-2130-2016 — The System 83 Plus, Endoscope Washer/Disinfector Designed for the simultaneous reprocessing of up to two flexible submersible endoscopes that are used in the gastrointestinal and/or pulmonary tracts.
- Z-0426-2014 — Custom Ultrasonics System 83 Plus 2 and Plus 9 Endoscope Washer/Disinfector.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Custom Ultrasonics, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.