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

Vivo 45 LS

K Number: K232365 · Decision Dec 19, 2025
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
1
Review Days
865

Basic Information

Device Name
Vivo 45 LS
K Number
K232365
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Oconnell Regulatory Consultants, Inc.
Date Received
August 7, 2023
Decision Date
December 19, 2025
Product Code
CBK
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CBK Ventilator, Continuous, Facility Use

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