MEDIPOINT— 510(k) K982961

Substantially Equivalent

Medipoint , Ltd.

FDA 510(k) clearance K982961 for MEDIPOINT, Substantially Equivalent on 1999-06-07. Applicant: Medipoint , Ltd.. Device class: 2.

Clearance details

Applicant: Medipoint , Ltd.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1998-08-24
Decision date: 1999-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, 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.