510(k) K152344
K152344 is an FDA 510(k) premarket notification submitted by Randox Laboratories Limited for the device "Total Bilirubin". The FDA issued a decision of Substantially Equivalent on January 28, 2016. The device falls under product code JFM (Enzymatic Method, Bilirubin), a Class II device regulated under 21 CFR 862.1110. Randox Laboratories Limited has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 28, 2016
- Date Received
- August 19, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzymatic Method, Bilirubin
- Device Class
- Class II
- Regulation Number
- 862.1110
- Review Panel
- CH
- Submission Type