510(k) K230841
- Device
- NailLift
- Applicant
- Jps Corporation
- 510(k) number
- K230841
- Product code
- MQZ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2024-01-22
- Date received
- 2023-03-28
- Classification name
- Prosthesis, Nail
- Medical specialty
- Unknown
- Review panel
- Unknown
- Device class
- U
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- Yasuko Kida
- Address
- Toho Edogawabashi Bldg. 3f, 1-24-8 Sekiguchi, Bunkyo-Ku Tokyo JP 112-0014 112-0014
FDA Registration Numbers#
- 3027728077