510(k) K203839
K203839 is an FDA 510(k) premarket notification submitted by Itamar Medical , Ltd. for the device "WatchPAT200U (WP200U)". The FDA issued a decision of Substantially Equivalent on Mar 21, 2022. The device falls under product code MNR (Ventilatory Effort Recorder), a Class II device regulated under 21 CFR 868.2375. Itamar Medical , Ltd. has 16 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 21, 2022
- Date Received
- Dec 30, 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)