Medical Device Manufacturer · US , Lehi , UT

Plexus Yoga, LLC Dba Chirp - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
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Denied

Plexus Yoga, LLC Dba Chirp has 1 FDA 510(k) cleared medical devices. Based in Lehi, US.

Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Plexus Yoga, LLC Dba Chirp Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Plexus Yoga, LLC Dba Chirp
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