MEDAID— 510(k) K810841

Substantially Equivalent

C.V.I., Inc.

FDA 510(k) clearance K810841 for MEDAID, Substantially Equivalent on 1981-06-12. Applicant: C.V.I., Inc.. Device class: 2.

Clearance details

Applicant: C.V.I., Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1981-03-27
Decision date: 1981-06-12
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.