Last synced on 25 January 2026 at 3:41 am

DENLASER, MODEL 800

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003541
510(k) Type
Traditional
Applicant
CAO Group, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2001
Days to Decision
70 days
Submission Type
Summary

DENLASER, MODEL 800

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003541
510(k) Type
Traditional
Applicant
CAO Group, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2001
Days to Decision
70 days
Submission Type
Summary