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PERIOLASE ND:YAG DENTAL LASER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014272
510(k) Type
Traditional
Applicant
Millennium Dental Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2002
Days to Decision
90 days
Submission Type
Summary

PERIOLASE ND:YAG DENTAL LASER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014272
510(k) Type
Traditional
Applicant
Millennium Dental Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2002
Days to Decision
90 days
Submission Type
Summary