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FDA 510(k)

MENTOR PERCUTANEOUS MALECOT NEPHROSTOMY SET

K-Number: K850287 · 1985-03-07

ApplicantMentor Corp.
Decision Date1985-03-07
Product CodeLJE
DecisionSubstantially Equivalent

Device Summary

MENTOR PERCUTANEOUS MALECOT NEPHROSTOMY SET is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 1985-03-07 under 510(k) number K850287. The device is classified under product code LJE. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENTOR PERCUTANEOUS MALECOT NEPHROSTOMY SET?

MENTOR PERCUTANEOUS MALECOT NEPHROSTOMY SET is a medical device that received FDA 510(k) clearance on 1985-03-07. The listed applicant is Mentor Corp.. The 510(k) number is K850287.

When did MENTOR PERCUTANEOUS MALECOT NEPHROSTOMY SET receive FDA 510(k) clearance?

MENTOR PERCUTANEOUS MALECOT NEPHROSTOMY SET received FDA 510(k) clearance on 1985-03-07, under 510(k) number K850287.

Who is the listed applicant for MENTOR PERCUTANEOUS MALECOT NEPHROSTOMY SET?

The FDA 510(k) record lists Mentor Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MENTOR PERCUTANEOUS MALECOT NEPHROSTOMY SET?

The FDA product code for MENTOR PERCUTANEOUS MALECOT NEPHROSTOMY SET is LJE.

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Other records listing Mentor Corp. 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.

K130813MENTOR CPX 4 BREAST TISSUE EXPANDERS AND MENTOR CPX 4 WITH SUTURE TABS BREAST TISSUE EXPANDERSK053414MENTOR NOVASILK MESHK050008MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETERK042851MENTOR OBTAPE TRANS-OBTURATOR SURGICAL KITK040959MENTOR GENESIS PENILE PROSTHESISK031767MENTOR OBTAPE TRANS-OBTURATOR TAPE

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Related Devices (Code: LJE)

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.

K250448Disposable Percutaneous Nephrostomy Dilatation KitShenzhen Trious Medical Technology Co., Ltd.K222705Introducer NeedleYoucare Technology Co.,Ltd. (Wuhan)K211911Kolibri Percutaneous Nephrostomy Catheters, Kolibri Percutaneous Nephrostomy Kits, Kolibri Direct Puncture SetsColoplast Corp.K201165In-Ka Percutaneous Balloon Dilatation Catheters, Amplatz SheathColoplast Corp.K191498Cook-Cope Loop Nephrostomy Set, Ultrathane Nephrostomy Set with Mac-Loc, Ultrathane Suprapubic Set with Mac-LocCook IncorporatedK190903Lawson Retrograde Nephrostomy Wire Puncture SetCook Incorporated

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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