CDI (TM) SYSTEM 100 MONITORING SYSTEM— 510(k) K902654

Name: FDA 510(k) clearance K902654
Creator: U.S. Food and Drug Administration
Published: 1990-11-05

Substantially Equivalent

3M Health Care, Ltd.

FDA 510(k) clearance K902654 for CDI (TM) SYSTEM 100 MONITORING SYSTEM, Substantially Equivalent on 1990-11-05. Applicant: 3M Health Care, Ltd.. Device class: 2.

Clearance details

Applicant: 3M Health Care, Ltd.
Product code: Code DTY
Device class: Class 2
Regulation: 21 CFR 870.4410
Advisory panel: Cardiovascular
Date received: 1990-06-15
Decision date: 1990-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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