Medical Device Manufacturer · US , Palo Alto , CA

Carbylan Biosurgery - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006
2
Total
2
Cleared
0
Denied

Carbylan Biosurgery has 2 FDA 510(k) cleared medical devices. Based in Palo Alto, US.

Historical record: 2 cleared submissions from 2006 to 2007. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Carbylan Biosurgery Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Carbylan Biosurgery

2 devices
1-2 of 2
Cleared Mar 15, 2007
ADVACOAT SINUS GEL AND STENT
K070496 · LYA
Ear, Nose, Throat · 23d
Cleared Dec 04, 2006
ADVACOAT SINUS GEL, MODEL 9100, ADVA SINUS STENT, MODEL 9200
K063308 · LYA
Ear, Nose, Throat · 32d
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