FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

IPL Hair Removal Device, Model(s): FY-B505AL, FY-B505AG, FY-B505BL, FY-B505BG, FY-B507AL, FY-B507AG, FY-B507BL, FY-B507BG, FY-B508AL, FY-B508AG, FY-B508BL, FY-B508BG, FY-B509AL, FY-B509AG, FY-B509BL, FY-B509BG

K Number: K230549 · Decision Apr 25, 2023
Classifications
1
FEI Numbers
90
Registration Numbers
91
Same Product Code
161
Applicant Total
2
Review Days
56

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Basic Information

Device Name
IPL Hair Removal Device, Model(s): FY-B505AL, FY-B505AG, FY-B505BL, FY-B505BG, FY-B507AL, FY-B507AG, FY-B507BL, FY-B507BG, FY-B508AL, FY-B508AG, FY-B508BL, FY-B508BG, FY-B509AL, FY-B509AG, FY-B509BL, FY-B509BG
K Number
K230549
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
Shenzhen Xiazhifeng Electronic Co., Ltd.
Date Received
February 28, 2023
Decision Date
April 25, 2023
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OHT), ordered by most recent decision date.

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Other Clearances by Shenzhen Xiazhifeng Electronic Co., Ltd.

K Number Device Name
K260594 IPL Hair Removal Device (FL-B505AG, FL-B505AP, FL-B505AM, FL-B507AG, FL-B507AP, FL-B507AM, FL-B508AG, FL-B508AP, FL-B508AM, FL-B509AG, FL-B509AP, FL-B509AM, FL-B510G, FL-B510P, FL-B510M, FL-B511G, FL-B511P, FL-B511M, FL-B512AG, FL-B512AP, FL-B512AM, FL-B513AG, FL-B513AP, FL-B513AM)