IF-II (TM), MODEL 9800— 510(k) K883462

Substantially Equivalent

Medical Devices, Inc.

FDA 510(k) clearance K883462 for IF-II (TM), MODEL 9800, Substantially Equivalent on 1989-05-24. Applicant: Medical Devices, Inc.. Device class: 2.

Clearance details

Applicant: Medical Devices, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1988-08-15
Decision date: 1989-05-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.