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FDA 510(k)

Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector

K-Number: K170955 · 2017-07-03

ApplicantSurgical Instrument Service and Savings Inc.(Dba Medline Ren
Decision Date2017-07-03
Product CodeNLQ
DecisionSubstantially Equivalent

Device Summary

Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector is a medical device manufactured by Surgical Instrument Service and Savings Inc.(Dba Medline Ren. It received FDA 510(k) clearance on 2017-07-03 under approval number K170955. The device is classified under product code NLQ. FDA Decision: Substantially Equivalent.

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 2017-07-03. It is manufactured by Surgical Instrument Service and Savings Inc.(Dba Medline Ren. The 510(k) number is K170955.

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 2017-07-03, under approval number K170955.

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.(Dba Medline Ren.

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.

Other Devices by Surgical Instrument Service and Savings Inc.(Dba Medline Ren

K153745Medline ReNewal Reprocessed LigaSure Impact Open Sealer/Divider K151617Livewire Electrophysiology Catheter K182588Medline ReNewal Reprocessed LigaSure Maryland Jaw Sealer/Divider K193563Medline ReNewal Reprocessed Harmonic ACE+7 Shears K241224Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Auto ID Technology (BD710DF282CT, BD710DF282RTS, BD710FJ282RTS, BD710FJ282CT)

Related Devices (Code: NLQ)

K151405Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue TechnologySurgical Instrument Services and Savings(Dba Medline Renewal K170456Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue TechnologyStryker Sustainability Solutions K161693Reprocessed HARMONIC ACE+7, 5 mm Diameter Shears with Advanced HemostasisStryker Sustainability Solutions K173627Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic DissectorSurgical Instrument Service and Savings, Inc. K190610Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue TechnologySterilmed, Inc. K182272Reprocessed HARMONIC ACE+ 7 Shears with Advanced HemostasisSterilmed, Inc.

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.

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