FDA 510(k)

VERTEX PERCUTANEOUS PUNCTURE NEEDLE

K-Number: K822596 · 1982-09-21

Decision Date1982-09-21

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

VERTEX PERCUTANEOUS PUNCTURE NEEDLE 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 1982-09-21 under 510(k) number K822596. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERTEX PERCUTANEOUS PUNCTURE NEEDLE?

VERTEX PERCUTANEOUS PUNCTURE NEEDLE is a medical device that received FDA 510(k) clearance on 1982-09-21. The listed applicant is Vertex Medical Corp.. The 510(k) number is K822596.

When did VERTEX PERCUTANEOUS PUNCTURE NEEDLE receive FDA 510(k) clearance?

VERTEX PERCUTANEOUS PUNCTURE NEEDLE received FDA 510(k) clearance on 1982-09-21, under 510(k) number K822596.

Who is the listed applicant for VERTEX PERCUTANEOUS PUNCTURE NEEDLE?

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 VERTEX PERCUTANEOUS PUNCTURE NEEDLE?

The FDA product code for VERTEX PERCUTANEOUS PUNCTURE NEEDLE is DQO.

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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.