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FDA 510(k)

PORGES NASOBILIARY DRAIN

K-Number: K896376 · 1990-01-22

ApplicantPorges Corp.
Decision Date1990-01-22
Product CodeFGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PORGES NASOBILIARY DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is Porges Corp.. It received FDA 510(k) clearance on 1990-01-22 under 510(k) number K896376. The device is classified under product code FGE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORGES NASOBILIARY DRAIN?

PORGES NASOBILIARY DRAIN is a medical device that received FDA 510(k) clearance on 1990-01-22. The listed applicant is Porges Corp.. The 510(k) number is K896376.

When did PORGES NASOBILIARY DRAIN receive FDA 510(k) clearance?

PORGES NASOBILIARY DRAIN received FDA 510(k) clearance on 1990-01-22, under 510(k) number K896376.

Who is the listed applicant for PORGES NASOBILIARY DRAIN?

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

What is the FDA product code for PORGES NASOBILIARY DRAIN?

The FDA product code for PORGES NASOBILIARY DRAIN is FGE.

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 Porges Corp. 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.

View all 18 devices →

Related Devices (Code: FGE)

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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