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

AEROSOL INHALATION MONITOR

K Number: K893665 · Decision Aug 21, 1989
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
17
Review Days
98

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Basic Information

Device Name
AEROSOL INHALATION MONITOR
K Number
K893665
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Vitalograph , Ltd.
Date Received
May 15, 1989
Decision Date
August 21, 1989
Product Code
BWF
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
BWF Spirometer, Therapeutic (Incentive)

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Other Clearances by Vitalograph , Ltd.

K Number Device Name
K253293 VitaloJAK Clinic (Model 7100)
K950854 VITALOGRAPH 2110 SOFTWARE INTERFACE
K925085 ESCORT SPIROMETER
K930085 VITALOGRAPH DATA STORAGE SPIROMETER
K912412 VITALOGRAPH SPIROTRAC III
K892524 VITALOGRAPH-BREATHCO MONITOR
K873562 VITALOGRAPH-ALPHA
K874892 VITALOGRAPH-EC60 HYDROGEN MONITOR
K863420 VITALOGRAPH EC-50 CARBON MONOXIDE MONITOR
K860949 DUAL-AID
Search all 17 clearances from Vitalograph , Ltd. →