FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

SILK'N FLASH N GO

K Number: K103184 · Decision Nov 10, 2010
Classifications
1
FEI Numbers
90
Registration Numbers
91
Same Product Code
161
Applicant Total
15
Review Days
12

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Basic Information

Device Name
SILK'N FLASH N GO
K Number
K103184
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Home Skinovations , Ltd.
Date Received
October 29, 2010
Decision Date
November 10, 2010
Product Code
OHT
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
OHT Light Based Over-The-Counter Hair Removal

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Other Clearances by Home Skinovations , Ltd.

K Number Device Name
K214078 Silk’n Toothwave
DEN190039 ToothWave™
K180279 Silk'n MODEL H5003 device
K171433 Silk'n Infinity
K162784 Silk'n HST
K152087 HeatLux Pro II
K150175 HeatLux Pro I
K141242 GLIDE DEVICE
K131870 GLIDE DEVICE
K121435 SILKN BLUE
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