MSI PROCEDURE KIT— 510(k) K944226

Substantially Equivalent

Msi, Inc.

FDA 510(k) clearance K944226 for MSI PROCEDURE KIT, Substantially Equivalent on 1995-06-21. Applicant: Msi, Inc.. Device class: 2.

Clearance details

Applicant: Msi, Inc.
Product code: Code DOX
Device class: Class 2
Regulation: 21 CFR 862.3550
Advisory panel: Clinical Toxicology
Date received: 1994-08-30
Decision date: 1995-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarpon Springs, FL, US

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