KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR— 510(k) K851627

Name: FDA 510(k) clearance K851627
Creator: U.S. Food and Drug Administration
Published: 1985-11-08

Substantially Equivalent

Eaton Medical Group

FDA 510(k) clearance K851627 for KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR, Substantially Equivalent on 1985-11-08. Applicant: Eaton Medical Group. Device class: 2.

Clearance details

Applicant: Eaton Medical Group
Product code: Code DRW
Device class: Class 2
Regulation: 21 CFR 870.2350
Advisory panel: Cardiovascular
Date received: 1985-04-18
Decision date: 1985-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eaton, MI, US

Download summary PDF View on FDA.gov ↗

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