Last synced on 25 April 2025 at 11:05 pm

MEDLITE Q-SWITCHED ND:YAG LASER REPLACED BY THE MEDLITE C3 Q-SWTICHED ND:YAG LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011677
510(k) Type
Special
Applicant
CONTINUUM ELECTRO-OPTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2001
Days to Decision
23 days
Submission Type
Summary

MEDLITE Q-SWITCHED ND:YAG LASER REPLACED BY THE MEDLITE C3 Q-SWTICHED ND:YAG LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011677
510(k) Type
Special
Applicant
CONTINUUM ELECTRO-OPTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2001
Days to Decision
23 days
Submission Type
Summary