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ULTRALIGHT II ND:YAG LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K041011
510(k) Type
Traditional
Applicant
SANDSTONE MEDICAL TECHNOLOGIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2004
Days to Decision
238 days
Submission Type
Summary

ULTRALIGHT II ND:YAG LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K041011
510(k) Type
Traditional
Applicant
SANDSTONE MEDICAL TECHNOLOGIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2004
Days to Decision
238 days
Submission Type
Summary