510(k) K180566
K180566 is an FDA 510(k) premarket notification submitted by Ascom Sweden AB for the device "Unite Connect for Clinical Systems". The FDA issued a decision of Substantially Equivalent on Apr 3, 2018. The device falls under product code MSX (System, Network And Communication, Physiological Monitors), a Class II device regulated under 21 CFR 870.2300.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 3, 2018
- Date Received
- Mar 5, 2018
- Clearance Type
- Special
- 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
- 510(k)