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FDA 510(k)

NES REPROCESSED ENDOSCOPIC TROCAR

K-Number: K060676 · 2007-09-07

ApplicantNortheast Scientific, Inc.
Decision Date2007-09-07
Product CodeNLM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NES REPROCESSED ENDOSCOPIC TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Northeast Scientific, Inc.. It received FDA 510(k) clearance on 2007-09-07 under 510(k) number K060676. The device is classified under product code NLM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NES REPROCESSED ENDOSCOPIC TROCAR?

NES REPROCESSED ENDOSCOPIC TROCAR is a medical device that received FDA 510(k) clearance on 2007-09-07. The listed applicant is Northeast Scientific, Inc.. The 510(k) number is K060676.

When did NES REPROCESSED ENDOSCOPIC TROCAR receive FDA 510(k) clearance?

NES REPROCESSED ENDOSCOPIC TROCAR received FDA 510(k) clearance on 2007-09-07, under 510(k) number K060676.

Who is the listed applicant for NES REPROCESSED ENDOSCOPIC TROCAR?

The FDA 510(k) record lists Northeast Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NES REPROCESSED ENDOSCOPIC TROCAR?

The FDA product code for NES REPROCESSED ENDOSCOPIC TROCAR is NLM.

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Other records listing Northeast Scientific, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250592NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)K223026NES Reprocessed Eagle Eye Platinum RX Digital IVUS CatheterK220171NES Reprocessed 0.9mm Turbo Elite Laser Atherectomy CatheterK200195NES Reprocessed Visions PV .014P RX Digital IVUS CatheterK090661NES REPROCESSED VARICOSE VEIN RF CATHETER

Related Devices (Code: NLM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K201511Reprocessed Endoscopic Trocars and SleevesStryker Sustainability SolutionsK182828Medline ReNewal Reprocessed Carter-Thomason Needle Point Suture PasserSurgical Instrument Service and Savings, Inc.K172097Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar SleevesRenovo, Inc.K172093Reprocessed Covidien TrocarRenovo, Inc.K160740Medline ReNewal Reprocessed ENDOPATH XCEL Trocar with OPTIVIEW TechnologySurgical Instrument Service and Savings, Inc.K153258Medline ReNewal Reprocessed Versaport V2 Bladeless Optical TrocarsSurgical Instrument Service and Savings (Dba Medline Renewal

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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