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FLUSH DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833170
510(k) Type
Traditional
Applicant
TRANSAMERICA DELAVAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1984
Days to Decision
331 days

FLUSH DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833170
510(k) Type
Traditional
Applicant
TRANSAMERICA DELAVAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1984
Days to Decision
331 days