AM 706 ELECTROMYOGRAPH, STIM., NEURO., EXTERNAL— 510(k) K881196

Name: FDA 510(k) clearance K881196
Creator: U.S. Food and Drug Administration
Published: 1989-06-16

Substantially Equivalent

Biometer Intl. A/S

FDA 510(k) clearance K881196 for AM 706 ELECTROMYOGRAPH, STIM., NEURO., EXTERNAL, Substantially Equivalent on 1989-06-16. Applicant: Biometer Intl. A/S. Device class: 2.

Clearance details

Applicant: Biometer Intl. A/S
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1988-03-21
Decision date: 1989-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denmark, DK

Download summary PDF View on FDA.gov ↗

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