MYOLAB II, MODEL ML-200— 510(k) K862236

Substantially Equivalent

Motion Control, Inc.

FDA 510(k) clearance K862236 for MYOLAB II, MODEL ML-200, Substantially Equivalent on 1986-08-07. Applicant: Motion Control, Inc.. Device class: 2.

Clearance details

Applicant: Motion Control, Inc.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1986-06-11
Decision date: 1986-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, 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.