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180W CERELAS D 980NM DIODE LASER, MODEL D180

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083682
510(k) Type
Special
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2009
Days to Decision
29 days
Submission Type
Summary

180W CERELAS D 980NM DIODE LASER, MODEL D180

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083682
510(k) Type
Special
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2009
Days to Decision
29 days
Submission Type
Summary