FDA 510(k)

MUC-X

K-Number: K893204 · 1989-06-01

Decision Date1989-06-01

Product CodeBSY

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

MUC-X is the device name listed in this FDA 510(k) record. The listed applicant is Island Medical. It received FDA 510(k) clearance on 1989-06-01 under 510(k) number K893204. 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 MUC-X?

MUC-X is a medical device that received FDA 510(k) clearance on 1989-06-01. The listed applicant is Island Medical. The 510(k) number is K893204.

When did MUC-X receive FDA 510(k) clearance?

MUC-X received FDA 510(k) clearance on 1989-06-01, under 510(k) number K893204.

Who is the listed applicant for MUC-X?

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

What is the FDA product code for MUC-X?

The FDA product code for MUC-X is BSY.

Other records listing Island 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.

K893120KIT, INTRAVENOUS EXTENSION TUBING

Related Devices (Code: BSY)

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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.