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

SERVICE MANAGER SM40SE

K Number: K053464 · Decision Jun 6, 2006
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
74
Applicant Total
1
Review Days
175

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Basic Information

Device Name
SERVICE MANAGER SM40SE
K Number
K053464
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5070
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Conmed Integrated Systems, Canada, Ulc
Date Received
December 13, 2005
Decision Date
June 6, 2006
Product Code
FYD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FYD Apparatus, Exhaust, Surgical

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