Medical Device Manufacturer · US , Albuquerque , NM

Avanca Medical Devices, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2005
3
Total
3
Cleared
0
Denied

Avanca Medical Devices, Inc. has 3 FDA 510(k) cleared medical devices. Based in Albuquerque, US.

Historical record: 3 cleared submissions from 2005 to 2005. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Avanca Medical Devices, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Avanca Medical Devices, Inc.
3 devices
1-3 of 3
Cleared Nov 09, 2005
PROCEDUR-10
K052075 · FMF
General Hospital · 100d
Cleared Jan 21, 2005
PROCEDUR 10 SYRINGE DEVICE
K042486 · FMF
General Hospital · 130d
Cleared Jan 21, 2005
PROCEDUR SF SAFETY SYRINGE DEVICE
K042487 · MEG
General Hospital · 130d
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