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FDA 510(k)

MGN CONDUCTIVE CONNECTING TUBE, STERILE

K-Number: K821703 · 1982-06-22

Decision Date1982-06-22
Product CodeBYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MGN CONDUCTIVE CONNECTING TUBE, STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Mgn Medical Manufacturing, Inc.. It received FDA 510(k) clearance on 1982-06-22 under 510(k) number K821703. The device is classified under product code BYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MGN CONDUCTIVE CONNECTING TUBE, STERILE?

MGN CONDUCTIVE CONNECTING TUBE, STERILE is a medical device that received FDA 510(k) clearance on 1982-06-22. The listed applicant is Mgn Medical Manufacturing, Inc.. The 510(k) number is K821703.

When did MGN CONDUCTIVE CONNECTING TUBE, STERILE receive FDA 510(k) clearance?

MGN CONDUCTIVE CONNECTING TUBE, STERILE received FDA 510(k) clearance on 1982-06-22, under 510(k) number K821703.

Who is the listed applicant for MGN CONDUCTIVE CONNECTING TUBE, STERILE?

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

What is the FDA product code for MGN CONDUCTIVE CONNECTING TUBE, STERILE?

The FDA product code for MGN CONDUCTIVE CONNECTING TUBE, STERILE is BYY.

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 Mgn Medical Manufacturing, 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: BYY)

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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