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FDA 510(k)

THE POREX RETRACTOR TABLE

K-Number: K860503 · 1986-03-13

ApplicantPorex Medical
Decision Date1986-03-13
Product CodeFSE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE POREX RETRACTOR TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Porex Medical. It received FDA 510(k) clearance on 1986-03-13 under 510(k) number K860503. The device is classified under product code FSE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE POREX RETRACTOR TABLE?

THE POREX RETRACTOR TABLE is a medical device that received FDA 510(k) clearance on 1986-03-13. The listed applicant is Porex Medical. The 510(k) number is K860503.

When did THE POREX RETRACTOR TABLE receive FDA 510(k) clearance?

THE POREX RETRACTOR TABLE received FDA 510(k) clearance on 1986-03-13, under 510(k) number K860503.

Who is the listed applicant for THE POREX RETRACTOR TABLE?

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

What is the FDA product code for THE POREX RETRACTOR TABLE?

The FDA product code for THE POREX RETRACTOR TABLE is FSE.

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 Porex Medical 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.

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Related Devices (Code: FSE)

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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