Last synced on 25 April 2025 at 11:05 pm

CERALAS D 980 DIODE LASER SYSTEM, MODELS D15, D25, D50

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032863
510(k) Type
Traditional
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2004
Days to Decision
189 days
Submission Type
Summary

CERALAS D 980 DIODE LASER SYSTEM, MODELS D15, D25, D50

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032863
510(k) Type
Traditional
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2004
Days to Decision
189 days
Submission Type
Summary