510(k) K894927

SURGI SQUEEZ by Ethox Corp. — Product Code KZD

K894927 is an FDA 510(k) premarket notification submitted by Ethox Corp. for the device "SURGI SQUEEZ". The FDA issued a decision of Substantially Equivalent on September 11, 1989. The device falls under product code KZD (Infusor, Pressure, For I.V. Bags), a Class I device regulated under 21 CFR 880.5420. Ethox Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 11, 1989
Date Received
August 2, 1989
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