MODEL PMT850— 510(k) K070931

Substantially Equivalent

Promedtek, Inc.

FDA 510(k) clearance K070931 for MODEL PMT850, Substantially Equivalent on 2007-05-24. Applicant: Promedtek, Inc.. Device class: 2.

Clearance details

Applicant: Promedtek, Inc.
Product code: Code ILX
Device class: Class 2
Regulation: 21 CFR 890.5290
Advisory panel: Physical Medicine
Date received: 2007-04-03
Decision date: 2007-05-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.