NEURO-PULSER 2 TRANSCUTAN. ELEC. NERVE— 510(k) K831850

Name: FDA 510(k) clearance K831850
Creator: U.S. Food and Drug Administration
Published: 1983-07-19

Substantially Equivalent

Th Charters, Inc.

FDA 510(k) clearance K831850 for NEURO-PULSER 2 TRANSCUTAN. ELEC. NERVE, Substantially Equivalent on 1983-07-19. Applicant: Th Charters, Inc.. Device class: 2.

Clearance details

Applicant: Th Charters, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1983-06-09
Decision date: 1983-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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