AMPLIFIER OTRONA, MODEL N3A-EMG— 510(k) K772102

Name: FDA 510(k) clearance K772102
Creator: U.S. Food and Drug Administration
Published: 1977-11-21

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K772102 for AMPLIFIER OTRONA, MODEL N3A-EMG, Substantially Equivalent on 1977-11-21. Applicant: Honeywell, Inc.. Device class: 2.

Clearance details

Applicant: Honeywell, Inc.
Product code: Code GWL
Device class: Class 2
Regulation: 21 CFR 882.1835
Advisory panel: Neurology
Date received: 1977-11-07
Decision date: 1977-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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