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FDA 510(k)

VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM

K-Number: K981700 · 1998-05-29

ApplicantOrigin Medsystems, Inc.
Decision Date1998-05-29
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Origin Medsystems, Inc.. It received FDA 510(k) clearance on 1998-05-29 under 510(k) number K981700. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM?

VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM is a medical device that received FDA 510(k) clearance on 1998-05-29. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K981700.

When did VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM receive FDA 510(k) clearance?

VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM received FDA 510(k) clearance on 1998-05-29, under 510(k) number K981700.

Who is the listed applicant for VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM?

The FDA 510(k) record lists Origin Medsystems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM?

The FDA product code for VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM is GCJ.

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Related Devices (Code: GCJ)

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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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