Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector
K-Number: K173627 · 2018-07-12
Device Summary
Frequently Asked Questions
What is the Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector?
Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector is a medical device that received FDA 510(k) clearance on 2018-07-12. It is manufactured by Surgical Instrument Service and Savings, Inc.. The 510(k) number is K173627.
When was Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector approved by the FDA?
Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector received FDA 510(k) clearance on 2018-07-12, under approval number K173627.
What company makes Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector?
Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector is manufactured by Surgical Instrument Service and Savings, Inc..
What is the FDA product code for Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector?
The FDA product code for Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector is NLQ.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.