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CERALAS E 980NM DIODE LASER, MODELS E15/980 AND E30/980

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082263
510(k) Type
Special
Applicant
Biolitec, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2008
Days to Decision
77 days
Submission Type
Summary

CERALAS E 980NM DIODE LASER, MODELS E15/980 AND E30/980

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082263
510(k) Type
Special
Applicant
Biolitec, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2008
Days to Decision
77 days
Submission Type
Summary