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CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSIS

Page Type
Cleared 510(K)
510(k) Number
K964514
510(k) Type
Traditional
Applicant
Corpak, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/1998
Days to Decision
605 days
Submission Type
Statement

CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSIS

Page Type
Cleared 510(K)
510(k) Number
K964514
510(k) Type
Traditional
Applicant
Corpak, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/1998
Days to Decision
605 days
Submission Type
Statement