FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

Jac-Cell Medic testers

K Number: K170105 · Decision Feb 28, 2017
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
1
Review Days
47

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Basic Information

Device Name
Jac-Cell Medic testers
K Number
K170105
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jac-Cell Medic
Date Received
January 12, 2017
Decision Date
February 28, 2017
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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