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ACCESSOR PERIPHERAL DILATING GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K895179
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1990
Days to Decision
202 days

ACCESSOR PERIPHERAL DILATING GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K895179
510(k) Type
Traditional
Applicant
PERIPHERAL SYSTEMS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1990
Days to Decision
202 days