510(k) K900300
K900300 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "LYTENING 2Z LYTENING SYSTEM 31". The FDA issued a decision of Substantially Equivalent on Mar 1, 1990. The device falls under product code CEM (Electrode, Ion Specific, Potassium), a Class II device regulated under 21 CFR 862.1600. Baxter Healthcare Corp has 507 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 1, 1990
- Date Received
- Jan 22, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Electrode, Ion Specific, Potassium
- Device Class
- Class II
- Regulation Number
- 862.1600
- Review Panel
- CH
- Submission Type
- 510(k)