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FDA 510(k)

CURITY SILICONE NEPHROSTOMY CATHETER

K-Number: K842840 · 1984-10-04

ApplicantThe Kendal Co.
Decision Date1984-10-04
Product CodeLJE
DecisionSubstantially Equivalent

Device Summary

CURITY SILICONE NEPHROSTOMY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1984-10-04 under 510(k) number K842840. The device is classified under product code LJE. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY SILICONE NEPHROSTOMY CATHETER?

CURITY SILICONE NEPHROSTOMY CATHETER is a medical device that received FDA 510(k) clearance on 1984-10-04. The listed applicant is The Kendal Co.. The 510(k) number is K842840.

When did CURITY SILICONE NEPHROSTOMY CATHETER receive FDA 510(k) clearance?

CURITY SILICONE NEPHROSTOMY CATHETER received FDA 510(k) clearance on 1984-10-04, under 510(k) number K842840.

Who is the listed applicant for CURITY SILICONE NEPHROSTOMY CATHETER?

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

What is the FDA product code for CURITY SILICONE NEPHROSTOMY CATHETER?

The FDA product code for CURITY SILICONE NEPHROSTOMY CATHETER is LJE.

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Other records listing The Kendal Co. 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.

K000087MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FRK990500KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946CK991758MONOJECT INSULIN SYRINGEK970969KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SETK951488KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAPK942664KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM

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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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