510(k) K013750
K013750 is an FDA 510(k) premarket notification submitted by Bayer Diagnostics Corp. for the device "ADVIA 1650 CHOLINESTERASE ASSAY". The FDA issued a decision of Substantially Equivalent on January 18, 2002. The device falls under product code DIH (Colorimetry, Cholinesterase), a Class I device regulated under 21 CFR 862.3240. Bayer Diagnostics Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 18, 2002
- Date Received
- November 13, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Colorimetry, Cholinesterase
- Device Class
- Class I
- Regulation Number
- 862.3240
- Review Panel
- TX
- Submission Type