FDA 510(k)

VENOSCOPE

K-Number: K941035 · 1994-05-16

Decision Date1994-05-16

Product CodeHJN

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

VENOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Trinity Partners, LLC. It received FDA 510(k) clearance on 1994-05-16 under 510(k) number K941035. The device is classified under product code HJN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENOSCOPE?

VENOSCOPE is a medical device that received FDA 510(k) clearance on 1994-05-16. The listed applicant is Trinity Partners, LLC. The 510(k) number is K941035.

When did VENOSCOPE receive FDA 510(k) clearance?

VENOSCOPE received FDA 510(k) clearance on 1994-05-16, under 510(k) number K941035.

Who is the listed applicant for VENOSCOPE?

The FDA 510(k) record lists Trinity Partners, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENOSCOPE?

The FDA product code for VENOSCOPE is HJN.

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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.