FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DEMAND OXYGEN CONTROLLER

K Number: K833351 · Decision Mar 19, 1984
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
7
Applicant Total
35
Review Days
173

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Basic Information

Device Name
DEMAND OXYGEN CONTROLLER
K Number
K833351
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5350
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Healthdyne, Inc.
Date Received
September 28, 1983
Decision Date
March 19, 1984
Product Code
BZB
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
BZB Catheter, Nasal, Oxygen

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Other Clearances by Healthdyne, Inc.

K Number Device Name
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K922106 ALICE
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
K892006 HEALTHDYNE'S APNEA/HEART MONITOR, MODEL 900S
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