510(k) K771458

INFUSION ACCELERATOR by Terumo America, Inc. — Product Code KZD

K771458 is an FDA 510(k) premarket notification submitted by Terumo America, Inc. for the device "INFUSION ACCELERATOR". The FDA issued a decision of Substantially Equivalent on August 26, 1977. The device falls under product code KZD (Infusor, Pressure, For I.V. Bags), a Class I device regulated under 21 CFR 880.5420. Terumo America, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 26, 1977
Date Received
August 4, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Infusor, Pressure, For I.V. Bags
Device Class
Class I
Regulation Number
880.5420
Review Panel
HO
Submission Type