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ENDOBRUSH(TM) DEVICE; OMNIBRUSH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K897070
510(k) Type
Traditional
Applicant
INTL. CYTOBRUSH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1990
Days to Decision
262 days

ENDOBRUSH(TM) DEVICE; OMNIBRUSH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K897070
510(k) Type
Traditional
Applicant
INTL. CYTOBRUSH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1990
Days to Decision
262 days