510(k) K191225
K191225 is an FDA 510(k) premarket notification submitted by Rhythmlink International, LLC for the device "EEG Electrode Template". The FDA issued a decision of Substantially Equivalent on August 5, 2019. The device falls under product code GXY (Electrode, Cutaneous), a Class II device regulated under 21 CFR 882.1320. Rhythmlink International, LLC has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 5, 2019
- Date Received
- May 7, 2019
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrode, Cutaneous
- Device Class
- Class II
- Regulation Number
- 882.1320
- Review Panel
- NE
- Submission Type