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

TV-100

K Number: K173973 · Decision Jul 20, 2018
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
14
Review Days
203

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Basic Information

Device Name
TV-100
K Number
K173973
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio-Med Devices, Inc.
Date Received
December 29, 2017
Decision Date
July 20, 2018
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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Other Clearances by Bio-Med Devices, Inc.

K Number Device Name
K213948 OxyMinder
K942938 CROSSVENT-4 VENTILATOR
K896381 MVP-10 MRI INFANT VENTILATOR
K896380 IC-2A MRI ADULT/PEDIATRIC VENTILATOR
K873614 CBG CUFF MANOMETER
K871337 M-2 OXYGEN/TEMPERATURE MONITOR
K871336 M-1 PRESSURE MONITOR
K871139 M-10 VENTILATION MONITOR
K830230 PROGRAMMABLE VENTILATOR
K823861 ET-3 EMERGENCY TRANSPORT VENTILATOR
Search all 14 clearances from Bio-Med Devices, Inc. →