Last synced on 25 January 2026 at 3:41 am

CERALAS MULTIWAVELENGTH 980/1470NM DIODE LASER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090164
510(k) Type
Traditional
Applicant
Biolitec, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2009
Days to Decision
155 days
Submission Type
Summary

CERALAS MULTIWAVELENGTH 980/1470NM DIODE LASER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090164
510(k) Type
Traditional
Applicant
Biolitec, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2009
Days to Decision
155 days
Submission Type
Summary