RESPONSE SYSTEM, TN-3000— 510(k) K781743

Name: FDA 510(k) clearance K781743
Creator: U.S. Food and Drug Administration
Published: 1978-12-01

Substantially Equivalent

Tracor Instruments, Inc.

FDA 510(k) clearance K781743 for RESPONSE SYSTEM, TN-3000, Substantially Equivalent on 1978-12-01. Applicant: Tracor Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Tracor Instruments, Inc.
Product code: Code GWL
Device class: Class 2
Regulation: 21 CFR 882.1835
Advisory panel: Neurology
Date received: 1978-10-20
Decision date: 1978-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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