LymphaTech Mobile 3D Measuring Tool
FDA 510(k) clearance K251255 · decided 2025-07-22
Clearance details
- K-number
- K251255
- Device name
- LymphaTech Mobile 3D Measuring Tool
- Applicant
- Lymphatech, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2025-04-23
- Decision date
- 2025-07-22
- Days to decision
- 90 days
- Clearance type
- Traditional
- Product code
- SFG
- Device class
- 1
- Regulation number
- 878.4160
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Atlanta, GA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.