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GOOSEN SELF-LUBRICATING CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923848
510(k) Type
Traditional
Applicant
GOOSEN ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1994
Days to Decision
567 days
Submission Type
Statement

GOOSEN SELF-LUBRICATING CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923848
510(k) Type
Traditional
Applicant
GOOSEN ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1994
Days to Decision
567 days
Submission Type
Statement