510(k) K112790
K112790 is an FDA 510(k) premarket notification submitted by Axis-Shield Diagnostics, Ltd. for the device "AXIS-SHIELD 3-REAGENT HOMOCYSTEINE ASSAY FOR SYNCHRON". The FDA issued a decision of Substantially Equivalent on May 7, 2012. The device falls under product code LPS (Urinary Homocystine (Nonquantitative) Test System), a Class II device regulated under 21 CFR 862.1377. Axis-Shield Diagnostics, Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 7, 2012
- Date Received
- September 26, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Urinary Homocystine (Nonquantitative) Test System
- Device Class
- Class II
- Regulation Number
- 862.1377
- Review Panel
- CH
- Submission Type