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FDA 510(k)

KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTOR

K-Number: K951995 · 1995-05-24

ApplicantKarl Storz Endoskop GmbH
Decision Date1995-05-24
Product CodeKNY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Endoskop GmbH. It received FDA 510(k) clearance on 1995-05-24 under 510(k) number K951995. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTOR?

KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTOR is a medical device that received FDA 510(k) clearance on 1995-05-24. The listed applicant is Karl Storz Endoskop GmbH. The 510(k) number is K951995.

When did KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTOR receive FDA 510(k) clearance?

KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTOR received FDA 510(k) clearance on 1995-05-24, under 510(k) number K951995.

Who is the listed applicant for KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTOR?

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

What is the FDA product code for KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTOR?

The FDA product code for KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTOR is KNY.

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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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