FDA 510(k)

MS300

K-Number: K984021 · 1999-01-28

Decision Date1999-01-28

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

MS300 is the device name listed in this FDA 510(k) record. The listed applicant is Lsi Intl., Inc.. It received FDA 510(k) clearance on 1999-01-28 under 510(k) number K984021. 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 MS300?

MS300 is a medical device that received FDA 510(k) clearance on 1999-01-28. The listed applicant is Lsi Intl., Inc.. The 510(k) number is K984021.

When did MS300 receive FDA 510(k) clearance?

MS300 received FDA 510(k) clearance on 1999-01-28, under 510(k) number K984021.

Who is the listed applicant for MS300?

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

What is the FDA product code for MS300?

The FDA product code for MS300 is IPF.

Other records listing Lsi Intl., 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.

K002390QUANTUM INTERSEGMENTAL TRACTION TABLE 400, 401, 400H,401H K984113MS400 K970696S.P. 100 K933653MS 2500

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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.