FDA 510(k) Applications Submitted by DIASOL, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K020230 |
01/23/2002 |
DIASOL-BICARB |
DIASOL, INC. |
K020231 |
01/23/2002 |
DIASOL-ADDITIVES |
DIASOL, INC. |
K130511 |
02/27/2013 |
CITRISOL ACID CONCENTRATE |
DIASOL, INC. |
K010958 |
03/30/2001 |
FISTULOK FISTULA NEEDLE PROTECTION |
DIASOL, INC. |
K011003 |
04/04/2001 |
SAFESTING AND SAFESTING HUB |
DIASOL, INC. |
K011004 |
04/04/2001 |
NEEDLELOK HYPODERMIC NEEDLE PROTECTION |
DIASOL, INC. |
K992653 |
08/06/1999 |
SHELLY PROTECTED AV FISTULA NEEDLE |
DIASOL, INC. |
K992999 |
09/07/1999 |
DAISY PROTECTED SCALP VEIN SET |
DIASOL, INC. |
K993187 |
09/23/1999 |
SHELLY PROTECTED AV FISTULA NEEDLE |
DIASOL, INC. |
K993212 |
09/24/1999 |
DRYASOL ACID CONCENTRATE MIX |
DIASOL, INC. |
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