Last synced on 25 April 2025 at 11:05 pm

ULTRASONIC DENTAL PROPHYLAXIS UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791024
510(k) Type
Traditional
Applicant
LITTON DENTAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1979
Days to Decision
110 days

ULTRASONIC DENTAL PROPHYLAXIS UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791024
510(k) Type
Traditional
Applicant
LITTON DENTAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1979
Days to Decision
110 days