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FDA 510(k)

Cleveland Multiport Ventricular Catheter Set

K-Number: K161731 · 2017-03-27

ApplicantParker Hannifin Corp.
Decision Date2017-03-27
Product CodeHCA
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Cleveland Multiport Ventricular Catheter Set is the device name listed in this FDA 510(k) record. The listed applicant is Parker Hannifin Corp.. It received FDA 510(k) clearance on 2017-03-27 under 510(k) number K161731. The device is classified under product code HCA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cleveland Multiport Ventricular Catheter Set?

Cleveland Multiport Ventricular Catheter Set is a medical device that received FDA 510(k) clearance on 2017-03-27. The listed applicant is Parker Hannifin Corp.. The 510(k) number is K161731.

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

Cleveland Multiport Ventricular Catheter Set received FDA 510(k) clearance on 2017-03-27, under 510(k) number K161731.

Who is the listed applicant for Cleveland Multiport Ventricular Catheter Set?

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

What is the FDA product code for Cleveland Multiport Ventricular Catheter Set?

The FDA product code for Cleveland Multiport Ventricular Catheter Set is HCA.

Other records listing Parker Hannifin 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.

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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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