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PERCUTANEOUS GUIDEWIRE PLACEMENT SYRINGE 50505

Page Type
Cleared 510(K)
510(k) Number
K855089
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1986
Days to Decision
60 days

PERCUTANEOUS GUIDEWIRE PLACEMENT SYRINGE 50505

Page Type
Cleared 510(K)
510(k) Number
K855089
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1986
Days to Decision
60 days