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PRIMROSE FEMALE EXT. CATH OR EXT. URINARY DRAINAGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890072
510(k) Type
Traditional
Applicant
MEDIREACH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1989
Days to Decision
154 days

PRIMROSE FEMALE EXT. CATH OR EXT. URINARY DRAINAGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890072
510(k) Type
Traditional
Applicant
MEDIREACH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1989
Days to Decision
154 days