510(k) K884307

IVAC(R) VOLUMETRIC CONTROLLER - MODEL 262 by Y — Product Code LDR

K884307 is an FDA 510(k) premarket notification submitted by Y for the device "IVAC(R) VOLUMETRIC CONTROLLER - MODEL 262". The FDA issued a decision of Substantially Equivalent on November 1, 1988. The device falls under product code LDR (Controller, Infusion, Intravascular, Electronic), a Class II device regulated under 21 CFR 880.5725. Y has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 1, 1988
Date Received
October 13, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Controller, Infusion, Intravascular, Electronic
Device Class
Class II
Regulation Number
880.5725
Review Panel
HO
Submission Type