510(k) K121865
K121865 is an FDA 510(k) premarket notification submitted by ZOLL Medical Corporation for the device "ZOLL RESCUENET 12-LEAD". The FDA issued a decision of Substantially Equivalent on November 20, 2012. The device falls under product code MSX (System, Network And Communication, Physiological Monitors), a Class II device regulated under 21 CFR 870.2300. ZOLL Medical Corporation has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 20, 2012
- Date Received
- June 26, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Network And Communication, Physiological Monitors
- Device Class
- Class II
- Regulation Number
- 870.2300
- Review Panel
- CV
- Submission Type