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DIODENT MICRO DENTAL LASER SYSTEM, MODELS 810 AND 980

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063384
510(k) Type
Traditional
Applicant
HOYA CONBIO, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2007
Days to Decision
128 days
Submission Type
Summary

DIODENT MICRO DENTAL LASER SYSTEM, MODELS 810 AND 980

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063384
510(k) Type
Traditional
Applicant
HOYA CONBIO, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2007
Days to Decision
128 days
Submission Type
Summary