SCX-10 SINGLE CHANNEL RECORDER ACCESS. FOR G-2000— 510(k) K851625

Name: FDA 510(k) clearance K851625
Creator: U.S. Food and Drug Administration
Published: 1985-11-19

Substantially Equivalent

Eaton Medical Group

FDA 510(k) clearance K851625 for SCX-10 SINGLE CHANNEL RECORDER ACCESS. FOR G-2000, Substantially Equivalent on 1985-11-19. 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: 1985-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eaton, MI, US

Download summary PDF View on FDA.gov ↗

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