S.P. 100— 510(k) K970696

Substantially Equivalent

Lsi Intl., Inc.

FDA 510(k) clearance K970696 for S.P. 100, Substantially Equivalent on 1997-03-18. Applicant: Lsi Intl., Inc.. Device class: 2.

Clearance details

Applicant: Lsi Intl., Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1997-02-25
Decision date: 1997-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Overland Park, KS, US

Download summary PDF View on FDA.gov ↗

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