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

COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES

K Number: K043238 · Decision Jul 6, 2005
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
507
Applicant Total
11
Review Days
226

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Basic Information

Device Name
COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES
K Number
K043238
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
868.5630
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Emg Technology Co., Ltd.
Date Received
November 22, 2004
Decision Date
July 6, 2005
Product Code
CAF
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
CAF Nebulizer (Direct Patient Interface)

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Other Clearances by Emg Technology Co., Ltd.

K Number Device Name
K112421 EMG SUCTION UNIT
K072634 EMG TRITON -COMP,MODEL NCA01-XXX SERIES
K063448 EMG AC/DC SUCTION UNIT
K062888 MIDDLE WHEEL DRIVE POWER CHAIR, CWD01
K052438 EMG HANDLE NEBULIZER NB02 SERIES
K043520 EMG CTA01-XXX SERIES PURO OXYGEN CONCENTRATOR
K042349 EMG MODEL SUA01 SUCTION UNIT
K033206 EPW FOLDABLE POWER WHEELCHAIR, EPW-03
K033204 ESG 4-WHEEL SCOOTER, ESG-03
K023148 EPW POWERED WHEELCHAIR, GP-201
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