510(k) K073592
K073592 is an FDA 510(k) premarket notification submitted by Mallinckrodt Inc., Liebel-Flarsheim Business for the device "OPTISTAR ELITE INJECTION SYSTEM". The FDA issued a decision of Substantially Equivalent on May 7, 2008. The device falls under product code DXT (Injector And Syringe, Angiographic), a Class II device regulated under 21 CFR 870.1650. Mallinckrodt Inc., Liebel-Flarsheim Business has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 7, 2008
- Date Received
- December 20, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Injector And Syringe, Angiographic
- Device Class
- Class II
- Regulation Number
- 870.1650
- Review Panel
- HO
- Submission Type