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MEDLINE RED RUBBER URETHRAL CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092250
510(k) Type
Traditional
Applicant
MEDLINE INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2010
Days to Decision
177 days
Submission Type
Statement

MEDLINE RED RUBBER URETHRAL CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092250
510(k) Type
Traditional
Applicant
MEDLINE INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2010
Days to Decision
177 days
Submission Type
Statement