510(k) K870991

IMED(R) MODEL 960A VOLUMETRIC INFUSION PUMP by Imed Corp. — Product Code FRN

K870991 is an FDA 510(k) premarket notification submitted by Imed Corp. for the device "IMED(R) MODEL 960A VOLUMETRIC INFUSION PUMP". The FDA issued a decision of Substantially Equivalent on June 4, 1987. The device falls under product code FRN (Pump, Infusion), a Class II device regulated under 21 CFR 880.5725. Imed Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 4, 1987
Date Received
March 11, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Infusion
Device Class
Class II
Regulation Number
880.5725
Review Panel
HO
Submission Type