MOSS LIMB LOAD MONITOR LM101-1— 510(k) K844202

Name: FDA 510(k) clearance K844202
Creator: U.S. Food and Drug Administration
Published: 1984-11-27

Substantially Equivalent

Moss Rehabilation Hospital

FDA 510(k) clearance K844202 for MOSS LIMB LOAD MONITOR LM101-1, Substantially Equivalent on 1984-11-27. Applicant: Moss Rehabilation Hospital. Device class: 1.

Clearance details

Applicant: Moss Rehabilation Hospital
Product code: Code IKE
Device class: Class 1
Regulation: 21 CFR 890.1615
Advisory panel: Physical Medicine
Date received: 1984-10-30
Decision date: 1984-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Philadelphia, PA, US

Download summary PDF View on FDA.gov ↗

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