MS300— 510(k) K984021

Substantially Equivalent

Lsi Intl., Inc.

FDA 510(k) clearance K984021 for MS300, Substantially Equivalent on 1999-01-28. Applicant: Lsi Intl., Inc.. Device class: 2.

Clearance details

Applicant: Lsi Intl., Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1998-11-12
Decision date: 1999-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Overland Park, KS, US

Download summary PDF View on FDA.gov ↗

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More clearances from Lsi Intl., Inc.

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Data sourced from openFDA. This site is unofficial and independent of the FDA.