PREAMPLIFIER MODEL 113— 510(k) K781289

Name: FDA 510(k) clearance K781289
Creator: U.S. Food and Drug Administration
Published: 1978-09-14

Substantially Equivalent

Princeton Applied Research Corp.

FDA 510(k) clearance K781289 for PREAMPLIFIER MODEL 113, Substantially Equivalent on 1978-09-14. Applicant: Princeton Applied Research Corp.. Device class: 2.

Clearance details

Applicant: Princeton Applied Research Corp.
Product code: Code GWL
Device class: Class 2
Regulation: 21 CFR 882.1835
Advisory panel: Neurology
Date received: 1978-07-27
Decision date: 1978-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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