FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Cogent™ Hemodynamic Monitoring System; Cogent™ HMS

K Number: K232048 · Decision Dec 20, 2023
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
176
Applicant Total
5
Review Days
163

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Basic Information

Device Name
Cogent™ Hemodynamic Monitoring System; Cogent™ HMS
K Number
K232048
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1435
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Icu Medical
Date Received
July 10, 2023
Decision Date
December 20, 2023
Product Code
DXG
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXG Computer, Diagnostic, Pre-Programmed, Single-Function

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