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

M-1 PRESSURE MONITOR

K Number: K871336 · Decision Jun 5, 1987
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
14
Review Days
63

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Basic Information

Device Name
M-1 PRESSURE MONITOR
K Number
K871336
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Bio-Med Devices, Inc.
Date Received
April 3, 1987
Decision Date
June 5, 1987
Product Code
CAP
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
CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

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Other Clearances by Bio-Med Devices, Inc.

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