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FDA 510(k)

MSI MAGNA-STYM

K-Number: K972055 · 1997-08-29

ApplicantMicrovas Systems, Inc.
Decision Date1997-08-29
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MSI MAGNA-STYM is the device name listed in this FDA 510(k) record. The listed applicant is Microvas Systems, Inc.. It received FDA 510(k) clearance on 1997-08-29 under 510(k) number K972055. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSI MAGNA-STYM?

MSI MAGNA-STYM is a medical device that received FDA 510(k) clearance on 1997-08-29. The listed applicant is Microvas Systems, Inc.. The 510(k) number is K972055.

When did MSI MAGNA-STYM receive FDA 510(k) clearance?

MSI MAGNA-STYM received FDA 510(k) clearance on 1997-08-29, under 510(k) number K972055.

Who is the listed applicant for MSI MAGNA-STYM?

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

What is the FDA product code for MSI MAGNA-STYM?

The FDA product code for MSI MAGNA-STYM is IPF.

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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.

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