HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3— 510(k) K003231

Name: FDA 510(k) clearance K003231
Creator: U.S. Food and Drug Administration
Published: 2001-01-12

Substantially Equivalent

Home Medical Services

FDA 510(k) clearance K003231 for HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3, Substantially Equivalent on 2001-01-12. Applicant: Home Medical Services. Device class: 2.

Clearance details

Applicant: Home Medical Services
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2000-10-17
Decision date: 2001-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, 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.