510(k) K050434
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