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FDA 510(k)

POLYVINYL CHLORIDE CANNULAS

K-Number: K844084 · 1984-10-30

Decision Date1984-10-30
Product CodeCAT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

POLYVINYL CHLORIDE CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Hudson Extrusions, Inc.. It received FDA 510(k) clearance on 1984-10-30 under 510(k) number K844084. The device is classified under product code CAT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLYVINYL CHLORIDE CANNULAS?

POLYVINYL CHLORIDE CANNULAS is a medical device that received FDA 510(k) clearance on 1984-10-30. The listed applicant is Hudson Extrusions, Inc.. The 510(k) number is K844084.

When did POLYVINYL CHLORIDE CANNULAS receive FDA 510(k) clearance?

POLYVINYL CHLORIDE CANNULAS received FDA 510(k) clearance on 1984-10-30, under 510(k) number K844084.

Who is the listed applicant for POLYVINYL CHLORIDE CANNULAS?

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

What is the FDA product code for POLYVINYL CHLORIDE CANNULAS?

The FDA product code for POLYVINYL CHLORIDE CANNULAS is CAT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Hudson Extrusions, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: CAT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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