510(k) K850258
K850258 is an FDA 510(k) premarket notification submitted by Bioclinical Systems, Inc. for the device "BCS POTASSIUM TURBIDIMETRIC TEST". The FDA issued a decision of Substantially Equivalent on February 7, 1985. The device falls under product code CEJ (Tetraphenyl Borate, Colorimetry, Potassium), a Class II device regulated under 21 CFR 862.1600. Bioclinical Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 7, 1985
- Date Received
- January 22, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tetraphenyl Borate, Colorimetry, Potassium
- Device Class
- Class II
- Regulation Number
- 862.1600
- Review Panel
- CH
- Submission Type