PRESSURE STOPCOCK/MANIFOLD


Device Classification Name

set, administration, intravascular

510(k) Number K960431
Device Name PRESSURE STOPCOCK/MANIFOLD
Applicant
SCIENTIFIC DEVICE MANUFACTURER LLC.
999 andersen drive, suite 120
san rafael, 
CA 
94901

Applicant Contact richard c ball
Correspondent
SCIENTIFIC DEVICE MANUFACTURER LLC.
999 andersen drive, suite 120
san rafael, 
CA 
94901

Correspodent Contact richard c ball
Regulation Number 880.5440
Classification Product Code
FPA  
Date Received 01/31/1996
Decision Date 10/29/1996
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No