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

MODEL 2120 SPIROSCREEN

K Number: K854403 · Decision Jan 14, 1986
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
227
Applicant Total
31
Review Days
75

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Basic Information

Device Name
MODEL 2120 SPIROSCREEN
K Number
K854403
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1840
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Gould, Inc.
Date Received
October 31, 1985
Decision Date
January 14, 1986
Product Code
BZG
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
BZG Spirometer, Diagnostic

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K850114 C/PES 9201, ECG STRESS TESTING SYS
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K843969 MODEL P23XL PHYSIOLOGICAL PRESSURE TRANSDUCER
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