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

EMERGENCY ASPIRATOR

K Number: K833785 · Decision Dec 22, 1983
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
17
Review Days
55

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Basic Information

Device Name
EMERGENCY ASPIRATOR
K Number
K833785
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Vitalograph , Ltd.
Date Received
October 28, 1983
Decision Date
December 22, 1983
Product Code
BTA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BTA Pump, Portable, Aspiration (Manual Or Powered)

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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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