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

PARAPAC 200D TRANSPORT, MODEL V200D

K Number: K030803 · Decision Sep 29, 2003
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
99
Applicant Total
19
Review Days
200

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Basic Information

Device Name
PARAPAC 200D TRANSPORT, MODEL V200D
K Number
K030803
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5925
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pneupac , Ltd.
Date Received
March 13, 2003
Decision Date
September 29, 2003
Product Code
BTL
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
BTL Ventilator, Emergency, Powered (Resuscitator)

Similar 510(k) Clearances

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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)
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
K820220 VENTILATOR MODELS
K792453 PNEUPAC OXYGEN THERAPY UNIT
Search all 19 clearances from Pneupac , Ltd. →