AUTOMOVE, MODEL AM800— 510(k) K032955

Substantially Equivalent

Danmeter A/S

FDA 510(k) clearance K032955 for AUTOMOVE, MODEL AM800, Substantially Equivalent on 2003-12-15. Applicant: Danmeter A/S. Device class: 2.

Clearance details

Applicant: Danmeter A/S
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2003-09-22
Decision date: 2003-12-15
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Odense C, DK

Download summary PDF View on FDA.gov ↗

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More clearances from Danmeter A/S

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