Last synced on 14 November 2025 at 11:06 pm

PERCUTANEOUS ARTERIAL/VENOUS CANNULA PLACEMENT KIT

Page Type
Cleared 510(K)
510(k) Number
K875353
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1988
Days to Decision
82 days

PERCUTANEOUS ARTERIAL/VENOUS CANNULA PLACEMENT KIT

Page Type
Cleared 510(K)
510(k) Number
K875353
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1988
Days to Decision
82 days