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PHOTEX30 DIODE LASER SERIES: 980, 810, 940

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092197
510(k) Type
Traditional
Applicant
BIOTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2009
Days to Decision
77 days
Submission Type
Summary

PHOTEX30 DIODE LASER SERIES: 980, 810, 940

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092197
510(k) Type
Traditional
Applicant
BIOTEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2009
Days to Decision
77 days
Submission Type
Summary