PC 2909A-HEALTH PULSE CONTROL STIMULATOR— 510(k) K830747

Name: FDA 510(k) clearance K830747
Creator: U.S. Food and Drug Administration
Published: 1983-05-30

Substantially Equivalent

J.A. Preston Corp.

FDA 510(k) clearance K830747 for PC 2909A-HEALTH PULSE CONTROL STIMULATOR, Substantially Equivalent on 1983-05-30. Applicant: J.A. Preston Corp.. Device class: 2.

Clearance details

Applicant: J.A. Preston Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1983-03-09
Decision date: 1983-05-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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