Diasol, Inc. is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diasol, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Diasol, Inc. has 10 FDA 510(k) cleared medical devices. Based in North Hollywood, US.
Historical record: 10 cleared submissions from 1999 to 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Diasol, Inc. Filter by specialty or product code using the sidebar.
Diasol, Inc. — FDA 510(k) Products and Clearance History
10 devices
Cleared
Feb 10, 2014
CITRISOL ACID CONCENTRATE
Gastroenterology & Urology
348d
Cleared
Oct 21, 2002
DIASOL-ADDITIVES
Gastroenterology & Urology
271d
Cleared
Apr 23, 2002
DIASOL-BICARB
Gastroenterology & Urology
90d
Cleared
May 24, 2001
NEEDLELOK HYPODERMIC NEEDLE PROTECTION
General Hospital
50d
Cleared
May 18, 2001
FISTULOK FISTULA NEEDLE PROTECTION
General Hospital
49d
Cleared
Apr 20, 2001
SAFESTING AND SAFESTING HUB
General Hospital
16d
Cleared
Nov 05, 1999
DAISY PROTECTED SCALP VEIN SET
General Hospital
59d
Cleared
Nov 05, 1999
SHELLY PROTECTED AV FISTULA NEEDLE
General Hospital
43d
Cleared
Oct 27, 1999
SHELLY PROTECTED AV FISTULA NEEDLE
Gastroenterology & Urology
82d
Cleared
Oct 22, 1999
DRYASOL ACID CONCENTRATE MIX
Gastroenterology & Urology
28d