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FDA 510(k)

Ventricular Catheter

K-Number: K200950 · 2020-05-08

ApplicantAesculap, Inc.
Decision Date2020-05-08
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Ventricular Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2020-05-08 under 510(k) number K200950. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ventricular Catheter?

Ventricular Catheter is a medical device that received FDA 510(k) clearance on 2020-05-08. The listed applicant is Aesculap, Inc.. The 510(k) number is K200950.

When did Ventricular Catheter receive FDA 510(k) clearance?

Ventricular Catheter received FDA 510(k) clearance on 2020-05-08, under 510(k) number K200950.

Who is the listed applicant for Ventricular Catheter?

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

What is the FDA product code for Ventricular Catheter?

The FDA product code for Ventricular Catheter is JXG.

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Other records listing Aesculap, Inc. as applicant

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K242762Aesculap Aicon® Series Container SystemK242003XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter SetK223596SQ.line KERRISONK214041Aesculap AICON ContainerK211572Aesculap Slim Clip ApplierK203739ELAN 4 Electro Motor System

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Related Devices (Code: JXG)

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.

K261004Codman® Distal Peritoneal Catheter, Barium Open End (82-1682); Codman® HOLTER® Peritoneal Catheter (SALMON Design) (82-1684)Integra Lifesciences Production CorporationK251598IntellidropBrainspace, Inc.K250636Sophy Mini Monopressure Valve (SM1)SophysaK252514EVAC-MRIPhasor Health, LLCK243531Codman Libertís Shunt Catheter with Bactiseal and Endexo TechnologyIntegra Lifesciences Production CorporationK243552Codman Libertís™ 1.5 mm EVD Catheter with Bactiseal® and Endexo® Technology with Luer Connection (821761); Codman Libertís™ 1.9 mm EVD Catheter with Bactiseal® and Endexo® Technology with Luer Connection (821762)Integra Lifesciences Production Corporation

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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