DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S— 510(k) K895473

Name: FDA 510(k) clearance K895473
Creator: U.S. Food and Drug Administration
Published: 1989-12-08

Substantially Equivalent

Medical Devices, Inc.

FDA 510(k) clearance K895473 for DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S, Substantially Equivalent on 1989-12-08. Applicant: Medical Devices, Inc.. Device class: 2.

Clearance details

Applicant: Medical Devices, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1989-09-11
Decision date: 1989-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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