510(k) K012340
K012340 is an FDA 510(k) premarket notification submitted by Bayer Corp. for the device "BAYER ADVIA SYSTEM; UNSATURATED IRON BINDING CAPACITY (UIBC)". The FDA issued a decision of Substantially Equivalent on October 1, 2001. The device falls under product code JMO (Ferrozine (Colorimetric) Iron Binding Capacity), a Class I device regulated under 21 CFR 862.1415. Bayer Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 1, 2001
- Date Received
- July 24, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ferrozine (Colorimetric) Iron Binding Capacity
- Device Class
- Class I
- Regulation Number
- 862.1415
- Review Panel
- CH
- Submission Type