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SILIVA EJECTOR/ORAL CAVITY EVACUATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864300
510(k) Type
Traditional
Applicant
ARDENT INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1986
Days to Decision
24 days

SILIVA EJECTOR/ORAL CAVITY EVACUATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864300
510(k) Type
Traditional
Applicant
ARDENT INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1986
Days to Decision
24 days