SCX-35 THREE CHANNEL ACCESS. FOR MODULE G-2000 ELE— 510(k) K851626

Name: FDA 510(k) clearance K851626
Creator: U.S. Food and Drug Administration
Published: 1985-06-26

Substantially Equivalent

Eaton Medical Group

FDA 510(k) clearance K851626 for SCX-35 THREE CHANNEL ACCESS. FOR MODULE G-2000 ELE, Substantially Equivalent on 1985-06-26. Applicant: Eaton Medical Group. Device class: 1.

Clearance details

Applicant: Eaton Medical Group
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1985-04-18
Decision date: 1985-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eaton, MI, US

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