Last synced on 14 November 2025 at 11:06 pm

LYMA Laser PRO

Page Type
Cleared 510(K)
510(k) Number
K243330
510(k) Type
Traditional
Applicant
LYMA Life Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/21/2025
Days to Decision
120 days
Submission Type
Summary

LYMA Laser PRO

Page Type
Cleared 510(K)
510(k) Number
K243330
510(k) Type
Traditional
Applicant
LYMA Life Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/21/2025
Days to Decision
120 days
Submission Type
Summary