Medical Device Manufacturer · US , Great Neck , NY

San UP S.A. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2001
2
Total
2
Cleared
0
Denied

San UP S.A. has 2 FDA 510(k) cleared medical devices. Based in Great Neck, US.

Historical record: 2 cleared submissions from 2001 to 2001. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by San UP S.A. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - San UP S.A.
2 devices
1-2 of 2
Cleared Jun 14, 2001
COMOACT ULTRASONIC NEBULIZER, MODEL 3060
K002543 · CAF
Anesthesiology · 302d
Cleared Mar 02, 2001
SAN UP S.A. NEBULIZER COMPRESSOR, WITH DISPOSABLE NEBULIZER, MODEL 3050
K002468 · BTI
Anesthesiology · 203d
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