FDA 510(k)

TUOHY-BORST ADAPTER W/SIDE ARM

K-Number: K823192 · 1982-12-30

Decision Date1982-12-30

Product CodeDXT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

TUOHY-BORST ADAPTER W/SIDE ARM is the device name listed in this FDA 510(k) record. The listed applicant is Vertex Medical Corp.. It received FDA 510(k) clearance on 1982-12-30 under 510(k) number K823192. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUOHY-BORST ADAPTER W/SIDE ARM?

TUOHY-BORST ADAPTER W/SIDE ARM is a medical device that received FDA 510(k) clearance on 1982-12-30. The listed applicant is Vertex Medical Corp.. The 510(k) number is K823192.

When did TUOHY-BORST ADAPTER W/SIDE ARM receive FDA 510(k) clearance?

TUOHY-BORST ADAPTER W/SIDE ARM received FDA 510(k) clearance on 1982-12-30, under 510(k) number K823192.

Who is the listed applicant for TUOHY-BORST ADAPTER W/SIDE ARM?

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

What is the FDA product code for TUOHY-BORST ADAPTER W/SIDE ARM?

The FDA product code for TUOHY-BORST ADAPTER W/SIDE ARM is DXT.

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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.