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EVOLVE HPD 980/ 1470NM MULTIWAVELENGTH DIODE LASER (EVOLVE DUAL)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120231
510(k) Type
Traditional
Applicant
BIOLITEC MEDICAL DEVICES, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2012
Days to Decision
90 days
Submission Type
Summary

EVOLVE HPD 980/ 1470NM MULTIWAVELENGTH DIODE LASER (EVOLVE DUAL)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120231
510(k) Type
Traditional
Applicant
BIOLITEC MEDICAL DEVICES, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2012
Days to Decision
90 days
Submission Type
Summary