FDA 510(k)

KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBES

K-Number: K944823 · 1994-11-02

Decision Date1994-11-02

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBES 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 1994-11-02 under 510(k) number K944823. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBES?

KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBES is a medical device that received FDA 510(k) clearance on 1994-11-02. The listed applicant is Karl Storz Endoskop GmbH. The 510(k) number is K944823.

When did KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBES receive FDA 510(k) clearance?

KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBES received FDA 510(k) clearance on 1994-11-02, under 510(k) number K944823.

Who is the listed applicant for KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBES?

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 INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBES?

The FDA product code for KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBES is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.