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FDA 510(k)

PERCUTANEOUS RETROGRADE NEPHROSTOMY

K-Number: K833762 · 1984-02-10

ApplicantVpi
Decision Date1984-02-10
Product CodeLJE
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS RETROGRADE NEPHROSTOMY is the device name listed in this FDA 510(k) record. The listed applicant is Vpi. It received FDA 510(k) clearance on 1984-02-10 under 510(k) number K833762. The device is classified under product code LJE. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUTANEOUS RETROGRADE NEPHROSTOMY?

PERCUTANEOUS RETROGRADE NEPHROSTOMY is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is Vpi. The 510(k) number is K833762.

When did PERCUTANEOUS RETROGRADE NEPHROSTOMY receive FDA 510(k) clearance?

PERCUTANEOUS RETROGRADE NEPHROSTOMY received FDA 510(k) clearance on 1984-02-10, under 510(k) number K833762.

Who is the listed applicant for PERCUTANEOUS RETROGRADE NEPHROSTOMY?

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

What is the FDA product code for PERCUTANEOUS RETROGRADE NEPHROSTOMY?

The FDA product code for PERCUTANEOUS RETROGRADE NEPHROSTOMY is LJE.

Related Clinical Trials

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.

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Other records listing Vpi 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.

K831875BALLOON DILATION HELICAL STONE EXTRACT

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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