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

DUAL-AID

K Number: K860949 · Decision May 6, 1986
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
56
Applicant Total
17
Review Days
55

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Basic Information

Device Name
DUAL-AID
K Number
K860949
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5110
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Vitalograph , Ltd.
Date Received
March 12, 1986
Decision Date
May 6, 1986
Product Code
CAE
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
CAE Airway, Oropharyngeal, Anesthesiology

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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
K893665 AEROSOL INHALATION MONITOR
K892524 VITALOGRAPH-BREATHCO MONITOR
K873562 VITALOGRAPH-ALPHA
K874892 VITALOGRAPH-EC60 HYDROGEN MONITOR
K863420 VITALOGRAPH EC-50 CARBON MONOXIDE MONITOR
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