Medical Device Manufacturer · US , Fort Myers , FL

Sims - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Sims Anesthesiology ✕

2 devices
1-2 of 2
Cleared Sep 17, 1997
SIMS 1ST RESPONSE MANUAL RESUSCITATOR, ADULT
K972283 · BTM
Anesthesiology · 90d
Cleared Jun 13, 1997
SIMS HYPERINFLATION BAG SYSTEM
K970785 · NHK
Anesthesiology · 101d
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