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PERITONEAL INTRODUCER & SHEATH

Page Type
Cleared 510(K)
510(k) Number
K771529
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1977
Days to Decision
8 days

PERITONEAL INTRODUCER & SHEATH

Page Type
Cleared 510(K)
510(k) Number
K771529
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1977
Days to Decision
8 days