Last synced on 25 April 2025 at 11:05 pm

OPTICA 25 ND:YAG DENTAL LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913839
510(k) Type
Traditional
Applicant
XINTEC CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1992
Days to Decision
200 days
Submission Type
Statement

OPTICA 25 ND:YAG DENTAL LASER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913839
510(k) Type
Traditional
Applicant
XINTEC CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1992
Days to Decision
200 days
Submission Type
Statement