510(k) K050434

SHL DISPOSABLE AUTOINJECTOR by Shl Medical, USA — Product Code KZH

K050434 is an FDA 510(k) premarket notification submitted by Shl Medical, USA for the device "SHL DISPOSABLE AUTOINJECTOR". The FDA issued a decision of Substantially Equivalent on June 24, 2005. The device falls under product code KZH (Introducer, Syringe Needle), a Class II device regulated under 21 CFR 880.6920. Shl Medical, USA has at least 1 other 510(k) clearance on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 24, 2005
Date Received
February 22, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Introducer, Syringe Needle
Device Class
Class II
Regulation Number
880.6920
Review Panel
HO
Submission Type