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PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK

Page Type
Cleared 510(K)
510(k) Number
K870374
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1987
Days to Decision
48 days

PERCUTANEOUS INTRODUCER W/SIDE PORT 3 WAY STOPCOCK

Page Type
Cleared 510(K)
510(k) Number
K870374
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1987
Days to Decision
48 days