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FDA 510(k)

DUNN VESSEL OCCLUDER-STERILE

K-Number: K851739 · 1985-09-27

ApplicantRichard J. Turner Assoc.
Decision Date1985-09-27
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DUNN VESSEL OCCLUDER-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Richard J. Turner Assoc.. It received FDA 510(k) clearance on 1985-09-27 under 510(k) number K851739. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUNN VESSEL OCCLUDER-STERILE?

DUNN VESSEL OCCLUDER-STERILE is a medical device that received FDA 510(k) clearance on 1985-09-27. The listed applicant is Richard J. Turner Assoc.. The 510(k) number is K851739.

When did DUNN VESSEL OCCLUDER-STERILE receive FDA 510(k) clearance?

DUNN VESSEL OCCLUDER-STERILE received FDA 510(k) clearance on 1985-09-27, under 510(k) number K851739.

Who is the listed applicant for DUNN VESSEL OCCLUDER-STERILE?

The FDA 510(k) record lists Richard J. Turner Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUNN VESSEL OCCLUDER-STERILE?

The FDA product code for DUNN VESSEL OCCLUDER-STERILE is DXC.

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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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