FDA 510(k), K790582, INTRAVASCULAR ADMINISTRATION SET Approval Letter

510(K) Number: K790582
Device Name: INTRAVASCULAR ADMINISTRATION SET
Manufacturer:
Device Classification Name: Set, Administration, Intravascular
Regulation Number: FPA
Classification Product Code: KXA
Date Received: 03/27/1979
Decision Date: 05/29/1979
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

Contents: Approval Letter

1 page