Last synced on 14 November 2025 at 11:06 pm

3B LASER NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K131797
510(k) Type
Traditional
Applicant
LIVETEC GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/2013
Days to Decision
114 days
Submission Type
Statement

3B LASER NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K131797
510(k) Type
Traditional
Applicant
LIVETEC GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/2013
Days to Decision
114 days
Submission Type
Statement