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

VENTILATOR MODELS

K Number: K820220 · Decision Feb 18, 1982
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
19
Review Days
22

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Basic Information

Device Name
VENTILATOR MODELS
K Number
K820220
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Pneupac , Ltd.
Date Received
January 27, 1982
Decision Date
February 18, 1982
Product Code
CBK
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
CBK Ventilator, Continuous, Facility Use

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Other Clearances by Pneupac , Ltd.

K Number Device Name
K040090 COMPPAC 200HD; CS12 POWER SUPPLY (AIRCRAFT/VECHILE); PS11 POWER SUPPLY (MAINS)
K030803 PARAPAC 200D TRANSPORT, MODEL V200D
K021841 COMPPAC VENTILATOR MODELS 200 & PS11 POWER SUPPLY/CHARGER
K020899 PARAPAC 200 MEDIC, MODEL P200, & PARAPAC 200D MEDIC, MODEL P200D
K960515 PARAPAC
K863410 PATIENT VALVE WITH AIR ENTRAINMENT
K862830 MODELS 2R AND 3R PNEUPAC VENTILATOR/RESUSCITATOR
K843737 PNEUPAC INSTANT ACTION VENTILATOR/RESUS
K832700 PNEU PAC VENTILATOR/RESUSCITATORS
K792453 PNEUPAC OXYGEN THERAPY UNIT
Search all 19 clearances from Pneupac , Ltd. →