SPEC IISX— 510(k) K831413

Substantially Equivalent

Medical Devices, Inc.

FDA 510(k) clearance K831413 for SPEC IISX, Substantially Equivalent on 1983-06-08. 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: 1983-05-02
Decision date: 1983-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.