FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

EMG TRITON -COMP,MODEL NCA01-XXX SERIES

K Number: K072634 · Decision Nov 19, 2008
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
73
Applicant Total
11
Review Days
428

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Basic Information

Device Name
EMG TRITON -COMP,MODEL NCA01-XXX SERIES
K Number
K072634
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.6250
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Emg Technology Co., Ltd.
Date Received
September 18, 2007
Decision Date
November 19, 2008
Product Code
BTI
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
Y

Classifications

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

Product Code Device Name
BTI Compressor, Air, Portable

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Other Clearances by Emg Technology Co., Ltd.

K Number Device Name
K112421 EMG SUCTION UNIT
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K062888 MIDDLE WHEEL DRIVE POWER CHAIR, CWD01
K052438 EMG HANDLE NEBULIZER NB02 SERIES
K043520 EMG CTA01-XXX SERIES PURO OXYGEN CONCENTRATOR
K043238 COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES
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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