Blue Sky Medical Group Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Blue Sky Medical Group Incorporated - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Blue Sky Medical Group Incorporated has 4 FDA 510(k) cleared medical devices. Based in Vista, US.
Historical record: 4 cleared submissions from 2004 to 2007. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Blue Sky Medical Group Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Blue Sky Medical Group Incorporated
4 devices
Cleared
Feb 05, 2007
VERSATILE 1 EZCARE WOUND VACUUM SYSTEM
General & Plastic Surgery
214d
Cleared
Aug 10, 2006
BLUESKY VISTA WOUND VACUUM SYSTEM, MODEL 100.0500
General & Plastic Surgery
86d
Cleared
Nov 04, 2005
MODIFICATION TO VERSATILE 1 WOUND VACUUM SYSTEM
General & Plastic Surgery
58d
Cleared
Nov 01, 2004
VERSATILE 1 WOUND VACUUM SYSTEM
General & Plastic Surgery
84d