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LASERLITE DIODE SURGICAL LASER

Page Type
Cleared 510(K)
510(k) Number
K981090
510(k) Type
Traditional
Applicant
LASERLITE, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1998
Days to Decision
26 days
Submission Type
Summary

LASERLITE DIODE SURGICAL LASER

Page Type
Cleared 510(K)
510(k) Number
K981090
510(k) Type
Traditional
Applicant
LASERLITE, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/1998
Days to Decision
26 days
Submission Type
Summary