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

FLOW SPIROMETER

K Number: K934502 · Decision Apr 4, 1994
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
79
Applicant Total
35
Review Days
202

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Basic Information

Device Name
FLOW SPIROMETER
K Number
K934502
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1860
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Healthdyne, Inc.
Date Received
September 14, 1993
Decision Date
April 4, 1994
Product Code
BZH
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
BZH Meter, Peak Flow, Spirometry

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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
K890150 H-3000 OXYGEN CONCENTRATOR
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