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

GOMCO SUCTION PUMP CABINET CHANGE

K Number: K810490 · Decision Mar 13, 1981
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
26
Review Days
17

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Basic Information

Device Name
GOMCO SUCTION PUMP CABINET CHANGE
K Number
K810490
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Allied Healthcare Products, Inc.
Date Received
February 24, 1981
Decision Date
March 13, 1981
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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K083507 BATTERY PACK FOR MCV100 AND MCV200 EMERGENCY VENTILATORS
K083385 MASS CASUALTY VENTILATORS, MODELS: MCV200 AND MCV200-B
K080063 MASS CASUALTY VENTILATOR, MODEL MCV100
K072214 PORTABLE VENTILATOR, MODEL EPV-100
K073171 RESUSCITATION TIMER, MODEL L770-CPR
K070636 AUTOVENT 4000 WITH CPAP
K070120 AUTOVENT MODEL 4000
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