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

M-2 OXYGEN/TEMPERATURE MONITOR

K Number: K871337 · Decision Jun 5, 1987
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
120
Applicant Total
14
Review Days
63

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
M-2 OXYGEN/TEMPERATURE MONITOR
K Number
K871337
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1720
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Bio-Med Devices, Inc.
Date Received
April 3, 1987
Decision Date
June 5, 1987
Product Code
CCL
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
CCL Analyzer, Gas, Oxygen, Gaseous-Phase

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CCL), ordered by most recent decision date.

View all

Other Clearances by Bio-Med Devices, Inc.

K Number Device Name
K213948 OxyMinder
K173973 TV-100
K942938 CROSSVENT-4 VENTILATOR
K896381 MVP-10 MRI INFANT VENTILATOR
K896380 IC-2A MRI ADULT/PEDIATRIC VENTILATOR
K873614 CBG CUFF MANOMETER
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. →