Medical Device Manufacturer · US , Salt Lake City , UT

Vela Operations USA - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023

Recent clearances: Great Basin Toxigenic C. difficile Direct Test (CDF2)

1
Total
1
Cleared
0
Denied

FDA 510(k) Regulatory Record - Vela Operations USA Microbiology

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