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DIAGNODENT 2190 WITH PERIODONTAL PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060080
510(k) Type
Special
Applicant
KAVO DENTAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2006
Days to Decision
29 days
Submission Type
Summary

DIAGNODENT 2190 WITH PERIODONTAL PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060080
510(k) Type
Special
Applicant
KAVO DENTAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2006
Days to Decision
29 days
Submission Type
Summary