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FDA 510(k)

KSEA SEMM TISSUR PUNCH

K-Number: K943053 · 1995-03-21

ApplicantKarl Storz Endoskop GmbH
Decision Date1995-03-21
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KSEA SEMM TISSUR PUNCH 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 1995-03-21 under 510(k) number K943053. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KSEA SEMM TISSUR PUNCH?

KSEA SEMM TISSUR PUNCH is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is Karl Storz Endoskop GmbH. The 510(k) number is K943053.

When did KSEA SEMM TISSUR PUNCH receive FDA 510(k) clearance?

KSEA SEMM TISSUR PUNCH received FDA 510(k) clearance on 1995-03-21, under 510(k) number K943053.

Who is the listed applicant for KSEA SEMM TISSUR PUNCH?

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 KSEA SEMM TISSUR PUNCH?

The FDA product code for KSEA SEMM TISSUR PUNCH is HET.

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Other records listing Karl Storz Endoskop GmbH 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.

K973068KSEA INSTRUMENT SET FOR SAPHENOUS VEIN HARVESTINGK961702KSEA VAPORIZATION ELECTRODESK953368LUER, JACKSON TRACHEA TUBES, LUER SPEAKING TRACHEA TUBESK943713TORCARS,CANNULAE,SHEATHS,OBTURATORSK951995KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTORK943435CHOLANGIOGRAPHY SET

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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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