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GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K895146
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1990
Days to Decision
150 days

GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K895146
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1990
Days to Decision
150 days