SMS-712NA— 510(k) K903085

Name: FDA 510(k) clearance K903085
Creator: U.S. Food and Drug Administration
Published: 1990-10-05

Substantially Equivalent

Toshiba America Medical Systems, In.C

FDA 510(k) clearance K903085 for SMS-712NA, Substantially Equivalent on 1990-10-05. Applicant: Toshiba America Medical Systems, In.C. Device class: 2.

Clearance details

Applicant: Toshiba America Medical Systems, In.C
Product code: Code GXW
Device class: Class 2
Regulation: 21 CFR 882.1240
Advisory panel: Neurology
Date received: 1990-07-12
Decision date: 1990-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tustin, CA, US

Download summary PDF View on FDA.gov ↗

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