Last synced on 14 November 2025 at 11:06 pm

PHOTEX DIODE LASER SERIES, MODELS 980, 810 AND 940

Page Type
Cleared 510(K)
510(k) Number
K060304
510(k) Type
Traditional
Applicant
BIOTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2006
Days to Decision
43 days
Submission Type
Summary

PHOTEX DIODE LASER SERIES, MODELS 980, 810 AND 940

Page Type
Cleared 510(K)
510(k) Number
K060304
510(k) Type
Traditional
Applicant
BIOTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2006
Days to Decision
43 days
Submission Type
Summary