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

MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON

K Number: K902785 · Decision Jul 13, 1990
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
174
Applicant Total
24
Review Days
17

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Basic Information

Device Name
MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON
K Number
K902785
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Aequitron Medical, Inc.
Date Received
June 26, 1990
Decision Date
July 13, 1990
Product Code
BZQ
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
BZQ Monitor, Breathing Frequency

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Other Clearances by Aequitron Medical, Inc.

K Number Device Name
K961972 MODEL AMI INFANT CENTRAL APHEA/HEART RATE MONITOR
K952880 MODEL LP-1000 VOLUME VENTILATOR
K944654 OXYGEN CONCENTRATION INDICATOR
K914424 MODEL 6213 REMOTE ALARM
K915381 PORTABLE OXYGEN GENERATOR
K911399 NASAL CPAP (CONTINUOUS POSITIVE AIR PRESSURE SYST)
K903020 RESPIRATION/HEART RATE MONITOR MODEL 9500/9550
K905244 MODEL LP6 VENTILATOR, MODIFICATION
K903010 CONTINUOUS VOLUME VENTILATOR MODEL LP10
K901656 MODEL 9200 RESPIRATION/HEART RATE MONITOR
Search all 24 clearances from Aequitron Medical, Inc. →