Sime Health, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sime Health, Ltd. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Sime Health, Ltd. has 11 FDA 510(k) cleared medical devices. Based in Seattle, US.
Historical record: 11 cleared submissions from 1991 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sime Health, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sime Health, Ltd.
11 devices
Cleared
Nov 15, 1995
SIME SURGICAL POWDERFREE
General Hospital
79d
Cleared
Nov 15, 1995
SIME POWDERFREE PLUS
General Hospital
78d
Cleared
Jun 16, 1995
AROMATIC CONDOM, ESSENTIALS, MI VIDA & JIFFI
Obstetrics & Gynecology
728d
Cleared
Jul 07, 1994
SPERMICIDAL LUBRIC. CONDOMS (ESSENTIALS, MI VIDA, JIFFI)
Obstetrics & Gynecology
384d
Cleared
Jul 07, 1994
COLORED CONDOMS (ESSENTIALS, MI VIDA, JIFFI)
Obstetrics & Gynecology
384d
Cleared
Jul 07, 1994
UNLUBRICATED CONDOM, ESSENTIALS, MI VIDA & JIFFI
Obstetrics & Gynecology
384d
Cleared
May 09, 1994
SIME SURGICAL LATEX GLOVE
General Hospital
76d
Cleared
Oct 15, 1993
SIME HEALTH SIME HYPOALLERGENIC
General Hospital
204d
Cleared
Dec 04, 1992
SIME HEALTH SIME POWDERFREE EXAMINATION GLOVES
General Hospital
437d
Cleared
Jun 01, 1992
JIFFI CONDOM (RUBBER) CONTRACEPTIVE
Obstetrics & Gynecology
280d
Cleared
Sep 19, 1991
SIME TRUFEEL
General Hospital
72d