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

VACPLUS SUCTION UNIT

K Number: K103535 · Decision Feb 24, 2011
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
76
Applicant Total
30
Review Days
85

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Basic Information

Device Name
VACPLUS SUCTION UNIT
K Number
K103535
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Apex Medical Corp.
Date Received
December 1, 2010
Decision Date
February 24, 2011
Product Code
JCX
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
JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered

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