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FDA 510(k)

MUCAID WITH SUCTION CATHETER AND EXTENSION TUBING

K-Number: K910908 · 1991-05-20

ApplicantVygon Corp.
Decision Date1991-05-20
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MUCAID WITH SUCTION CATHETER AND EXTENSION TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 1991-05-20 under 510(k) number K910908. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUCAID WITH SUCTION CATHETER AND EXTENSION TUBING?

MUCAID WITH SUCTION CATHETER AND EXTENSION TUBING is a medical device that received FDA 510(k) clearance on 1991-05-20. The listed applicant is Vygon Corp.. The 510(k) number is K910908.

When did MUCAID WITH SUCTION CATHETER AND EXTENSION TUBING receive FDA 510(k) clearance?

MUCAID WITH SUCTION CATHETER AND EXTENSION TUBING received FDA 510(k) clearance on 1991-05-20, under 510(k) number K910908.

Who is the listed applicant for MUCAID WITH SUCTION CATHETER AND EXTENSION TUBING?

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

What is the FDA product code for MUCAID WITH SUCTION CATHETER AND EXTENSION TUBING?

The FDA product code for MUCAID WITH SUCTION CATHETER AND EXTENSION TUBING is BSY.

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 Vygon 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 48 devices →

Related Devices (Code: BSY)

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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