FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
iHelmet Hair Growth System
K Number: K162782
·
Decision Apr 4, 2017
Classifications
1
FEI Numbers
67
Registration Numbers
67
Same Product Code
109
Applicant Total
3
Review Days
183
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Basic Information
- Device Name
- iHelmet Hair Growth System
- K Number
- K162782
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.5500
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Slinph Technologies Co., Ltd.
- Date Received
- October 3, 2016
- Decision Date
- April 4, 2017
- Product Code
- OAP
- Advisory Committee
- Physical Medicine
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| OAP | Laser, Comb, Hair | FDA class 2 | Physical Medicine |
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