510(k) K811661
K811661 is an FDA 510(k) premarket notification submitted by King Diagnostics, Inc. for the device "POTASSIUM TEST". The FDA issued a decision of Substantially Equivalent on June 25, 1981. The device falls under product code CEJ (Tetraphenyl Borate, Colorimetry, Potassium), a Class II device regulated under 21 CFR 862.1600. King Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 25, 1981
- Date Received
- June 15, 1981
- 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