Last synced on 14 November 2025 at 11:06 pm

LASER SYSTEM YELLOWSTAR

Page Type
Cleared 510(K)
510(k) Number
K013940
510(k) Type
Traditional
Applicant
ASCLEPION-MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2002
Days to Decision
89 days
Submission Type
Summary

LASER SYSTEM YELLOWSTAR

Page Type
Cleared 510(K)
510(k) Number
K013940
510(k) Type
Traditional
Applicant
ASCLEPION-MEDITEC AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2002
Days to Decision
89 days
Submission Type
Summary