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FDA 510(k)

VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM

K-Number: K041321 · 2004-07-09

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date2004-07-09
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 2004-07-09 under 510(k) number K041321. 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 VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM?

VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM is a medical device that received FDA 510(k) clearance on 2004-07-09. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K041321.

When did VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM receive FDA 510(k) clearance?

VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM received FDA 510(k) clearance on 2004-07-09, under 510(k) number K041321.

Who is the listed applicant for VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM?

The FDA product code for VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM is HET.

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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.

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