510(k) K894586

DALE I.V. IDENTIFIER; PRODUCT #1125 by Dale Medical Products, Inc. — Product Code KMK

K894586 is an FDA 510(k) premarket notification submitted by Dale Medical Products, Inc. for the device "DALE I.V. IDENTIFIER; PRODUCT #1125". The FDA issued a decision of Substantially Equivalent on August 15, 1989. The device falls under product code KMK (Device, Intravascular Catheter Securement), a Class I device regulated under 21 CFR 880.5210. Dale Medical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 15, 1989
Date Received
July 24, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Intravascular Catheter Securement
Device Class
Class I
Regulation Number
880.5210
Review Panel
HO
Submission Type