Last synced on 12 October 2025 at 8:21 pm

SONUS III

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K761246
510(k) Type
Traditional
Applicant
LITTON DENTAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1976
Days to Decision
3 days

SONUS III

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K761246
510(k) Type
Traditional
Applicant
LITTON DENTAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1976
Days to Decision
3 days