SPECIMEX DC— 510(k) K900740

Substantially Equivalent

Soredex Medical Systems

FDA 510(k) clearance K900740 for SPECIMEX DC, Substantially Equivalent on 1990-05-11. Applicant: Soredex Medical Systems. Device class: 2.

Clearance details

Applicant: Soredex Medical Systems
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 1990-02-16
Decision date: 1990-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Conroe, TX, 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.