LINASYS— 510(k) K071063

Substantially Equivalent

Pathfinder Therapeutics, Inc.

FDA 510(k) clearance K071063 for LINASYS, Substantially Equivalent on 2007-12-20. Applicant: Pathfinder Therapeutics, Inc.. Device class: 2.

Clearance details

Applicant: Pathfinder Therapeutics, Inc.
Product code: Code OEW
Device class: Class 2
Regulation: 21 CFR 882.4560
Advisory panel: Neurology
Date received: 2007-04-16
Decision date: 2007-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nashville, TN, US

Download summary PDF View on FDA.gov ↗

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More clearances from Pathfinder Therapeutics, Inc.

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