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KPP PERITONEAL DIALYSATE FILTER

Page Type
Cleared 510(K)
510(k) Number
K803275
510(k) Type
Traditional
Applicant
MILLIPORE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1981
Days to Decision
74 days

KPP PERITONEAL DIALYSATE FILTER

Page Type
Cleared 510(K)
510(k) Number
K803275
510(k) Type
Traditional
Applicant
MILLIPORE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1981
Days to Decision
74 days