Andrew Technologies, LLC is one of 19789 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Andrew Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: HYDRASOLVE LIPOPLASTY SYSTEM, HYDRASOLVE CONSOLE STERILE TREATMENT KIT REUSABLE CANNULA, 4MM DIA, 26 CM LENGTH, 3 APERTURE REUSABLE CANNULA, 4MM DIA,, PHASER LIPOPLASTY SYSTEM (DUR-01), PHASER DISPOSABLE KIT (DIS-01), PHASER WASTE COLLECTION KIT (WAS-01), PHASER CANNULAE
3
Total
3
Cleared
0
Denied
Andrew Technologies, LLC has 3 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 3 cleared submissions from 2010 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Andrew Technologies, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Andrew Technologies, LLC
3 devices
Cleared
Apr 18, 2013
HYDRASOLVE LIPOPLASTY SYSTEM
General & Plastic Surgery
86d
Cleared
Dec 13, 2012
HYDRASOLVE CONSOLE STERILE TREATMENT KIT REUSABLE CANNULA, 4MM DIA, 26 CM...
General & Plastic Surgery
234d
Cleared
Apr 12, 2010
PHASER LIPOPLASTY SYSTEM (DUR-01), PHASER DISPOSABLE KIT (DIS-01), PHASER...
General & Plastic Surgery
278d