Last synced on 25 April 2025 at 11:05 pm

CERALAS D/ 980NM FIBER-COUPLED DIODE LASER FAMILY, CERALAS E/ 980NM FIBER-COUPLED DIODE LASER FAMILY, CERALAS HPD/ 980NM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100726
510(k) Type
Traditional
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2010
Days to Decision
184 days
Submission Type
Summary

CERALAS D/ 980NM FIBER-COUPLED DIODE LASER FAMILY, CERALAS E/ 980NM FIBER-COUPLED DIODE LASER FAMILY, CERALAS HPD/ 980NM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100726
510(k) Type
Traditional
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/2010
Days to Decision
184 days
Submission Type
Summary