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EDM(R) INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K914979
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/1992
Days to Decision
315 days
Submission Type
Statement

EDM(R) INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K914979
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/1992
Days to Decision
315 days
Submission Type
Statement