510(k) K251255
- Device
- LymphaTech Mobile 3D Measuring Tool
- Applicant
- Lymphatech, Inc.
- 510(k) number
- K251255
- Product code
- SFG
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2025-07-22
- Date received
- 2025-04-23
- Regulation
- 878.4160
- Classification name
- Camera, Surgical, Measurement
- Medical specialty
- General, Plastic Surgery
- Review panel
- General, Plastic Surgery
- Device class
- 1
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- N
Related Records
Applicant Contact
- Contact
- Mike Weiler
- Address
- 976 Brady Ave. NW Suite 100 Atlanta GA US 30318 30318
FDA Registration Numbers
- 3031823375