510(k) K200654
K200654 is an FDA 510(k) premarket notification submitted by Dymedix Diagnostics, Inc. for the device "Rubicon SA System". The FDA issued a decision of Substantially Equivalent on Jul 22, 2020. The device falls under product code MNR (Ventilatory Effort Recorder), a Class II device regulated under 21 CFR 868.2375. Dymedix Diagnostics, Inc. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 22, 2020
- Date Received
- Mar 12, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ventilatory Effort Recorder
- Device Class
- Class II
- Regulation Number
- 868.2375
- Review Panel
- AN
- Submission Type
- 510(k)