SONIC PALPOMETER— 510(k) K060125

Substantially Equivalent

Palpometer Systems, Inc.

FDA 510(k) clearance K060125 for SONIC PALPOMETER, Substantially Equivalent on 2006-03-16. Applicant: Palpometer Systems, Inc.. Device class: 1.

Clearance details

Applicant: Palpometer Systems, Inc.
Product code: Code IKE
Device class: Class 1
Regulation: 21 CFR 890.1615
Advisory panel: Physical Medicine
Date received: 2006-01-18
Decision date: 2006-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Victoria, British Columbia, CA

Download summary PDF View on FDA.gov ↗

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