MODIFIED CASS SYSTEM— 510(k) K902488

Name: FDA 510(k) clearance K902488
Creator: U.S. Food and Drug Administration
Published: 1990-12-07

Substantially Equivalent

Medical Instrumentation & Diagnostics Corp.(Midco)

FDA 510(k) clearance K902488 for MODIFIED CASS SYSTEM, Substantially Equivalent on 1990-12-07. Applicant: Medical Instrumentation & Diagnostics Corp.(Midco). Device class: 2.

Clearance details

Applicant: Medical Instrumentation & Diagnostics Corp.(Midco)
Product code: Code KXK
Device class: Class 2
Regulation: 21 CFR 892.5730
Advisory panel: Radiology
Date received: 1990-05-30
Decision date: 1990-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Albuquerque, NM, US

Download summary PDF View on FDA.gov ↗

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