510(k) K202631
K202631 is an FDA 510(k) premarket notification submitted by Slinph Technologies Co., Ltd. for the device "iHelmet Laser Comb". The FDA issued a decision of Substantially Equivalent on Dec 8, 2020. The device falls under product code OAP (Laser, Comb, Hair), a Class II device regulated under 21 CFR 890.5500. Slinph Technologies Co., Ltd. has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 8, 2020
- Date Received
- Sep 11, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Laser, Comb, Hair
- Device Class
- Class II
- Regulation Number
- 890.5500
- Review Panel
- SU
- Submission Type
- 510(k)
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