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FDA 510(k)

TROCARS,CANNULAE,SHEATHS,OBTURATORS

K-Number: K943697 · 1994-09-14

ApplicantKarl Storz Endoskop GmbH
Decision Date1994-09-14
Product CodeODB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TROCARS,CANNULAE,SHEATHS,OBTURATORS 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 1994-09-14 under 510(k) number K943697. The device is classified under product code ODB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROCARS,CANNULAE,SHEATHS,OBTURATORS?

TROCARS,CANNULAE,SHEATHS,OBTURATORS is a medical device that received FDA 510(k) clearance on 1994-09-14. The listed applicant is Karl Storz Endoskop GmbH. The 510(k) number is K943697.

When did TROCARS,CANNULAE,SHEATHS,OBTURATORS receive FDA 510(k) clearance?

TROCARS,CANNULAE,SHEATHS,OBTURATORS received FDA 510(k) clearance on 1994-09-14, under 510(k) number K943697.

Who is the listed applicant for TROCARS,CANNULAE,SHEATHS,OBTURATORS?

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 TROCARS,CANNULAE,SHEATHS,OBTURATORS?

The FDA product code for TROCARS,CANNULAE,SHEATHS,OBTURATORS is ODB.

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Other records listing Karl Storz Endoskop GmbH as applicant

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K973068KSEA INSTRUMENT SET FOR SAPHENOUS VEIN HARVESTINGK961702KSEA VAPORIZATION ELECTRODESK953368LUER, JACKSON TRACHEA TUBES, LUER SPEAKING TRACHEA TUBESK943713TORCARS,CANNULAE,SHEATHS,OBTURATORSK951995KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTORK943053KSEA SEMM TISSUR PUNCH

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Related Devices (Code: ODB)

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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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