510(k) K880537

POLE, INTRAVENOUS by Ferguson Medical — Product Code FOX

K880537 is an FDA 510(k) premarket notification submitted by Ferguson Medical for the device "POLE, INTRAVENOUS". The FDA issued a decision of Substantially Equivalent on April 6, 1988. The device falls under product code FOX (Stand, Infusion), a Class I device regulated under 21 CFR 880.6990. Ferguson Medical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 6, 1988
Date Received
February 9, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stand, Infusion
Device Class
Class I
Regulation Number
880.6990
Review Panel
HO
Submission Type