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CURATIVE980 DIODE LASER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082445
510(k) Type
Traditional
Applicant
Oroscience, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2008
Days to Decision
51 days
Submission Type
Summary

CURATIVE980 DIODE LASER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082445
510(k) Type
Traditional
Applicant
Oroscience, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2008
Days to Decision
51 days
Submission Type
Summary