Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Medline ReNewal Reprocessed Endopath Endoscopic Instruments

K-Number: K152313 · 2016-01-06

ApplicantSurgical Instrument Services and Savings, Inc.
Decision Date2016-01-06
Product CodeNUJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Medline ReNewal Reprocessed Endopath Endoscopic Instruments is a medical device manufactured by Surgical Instrument Services and Savings, Inc.. It received FDA 510(k) clearance on 2016-01-06 under approval number K152313. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline ReNewal Reprocessed Endopath Endoscopic Instruments?

Medline ReNewal Reprocessed Endopath Endoscopic Instruments is a medical device that received FDA 510(k) clearance on 2016-01-06. It is manufactured by Surgical Instrument Services and Savings, Inc.. The 510(k) number is K152313.

When was Medline ReNewal Reprocessed Endopath Endoscopic Instruments approved by the FDA?

Medline ReNewal Reprocessed Endopath Endoscopic Instruments received FDA 510(k) clearance on 2016-01-06, under approval number K152313.

What company makes Medline ReNewal Reprocessed Endopath Endoscopic Instruments?

Medline ReNewal Reprocessed Endopath Endoscopic Instruments is manufactured by Surgical Instrument Services and Savings, Inc..

What is the FDA product code for Medline ReNewal Reprocessed Endopath Endoscopic Instruments?

The FDA product code for Medline ReNewal Reprocessed Endopath Endoscopic Instruments is NUJ.

Related Clinical Trials

NCT07568366 AI in Endoscopic Transsphenoidal Surgery NOT_YET_RECRUITING NCT05272046 Monopolar and Bipolar Current RFA Knife in POEM ACTIVE_NOT_RECRUITING

Other Devices by Surgical Instrument Services and Savings, Inc.

K162751Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/Divider K232130Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheter

Related Devices (Code: NUJ)

K161086Reprocessed Harmonic Shears with Adaptive Tissue Technology (36 cm), Reprocessed Harmonic Shears with Adaptive Tissue Technology (23cm)Sterilmed, Inc. K160333Medline ReNewal Reprocessed LigaSure Blunt Tip Open Sealer/DividerSurgical Instrument Service and Savings, Inc. K153745Medline ReNewal Reprocessed LigaSure Impact Open Sealer/DividerSurgical Instrument Service and Savings Inc.(Dba Medline Ren K152134Reprocessed Vessel SealerSterilmed, Inc. K172608Medline ReNewal Reprocessed Stryker SERF AS Energy ProbesSurgical Instrument Service and Savings, Inc. K171324Medline ReNewal Reprocessed ArthroCare ArthroWands and Smith & Nephew DyonicsSurgical Instrument Service and Savings, 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.

↑