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

HEALTHDYNE'S APNEA/HEART MONITOR, MODEL 900S

K Number: K892006 · Decision May 23, 1989
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
338
Applicant Total
35
Review Days
56

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Basic Information

Device Name
HEALTHDYNE'S APNEA/HEART MONITOR, MODEL 900S
K Number
K892006
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Healthdyne, Inc.
Date Received
March 28, 1989
Decision Date
May 23, 1989
Product Code
DRT
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

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Other Clearances by Healthdyne, Inc.

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K942357 H-500 ALLIANCE OXYGEN CONCENTRATOR
K934502 FLOW SPIROMETER
K924146 OH-500 OXYGEN CONCENTRATOR
K922623 NEBULIZER SYSTEM
K910118 DATA RECORDER
K903287 MODEL 900S APNEA/HEART MONITOR
K894030 MODEL 37 UTERINE CONTRACTION ACTIVITY MONITOR
K890150 H-3000 OXYGEN CONCENTRATOR
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