Rostam , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rostam , Ltd. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Rostam , Ltd. has 9 FDA 510(k) cleared medical devices. Based in Allendale, US.
Historical record: 9 cleared submissions from 1997 to 2010. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Rostam , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rostam , Ltd.
9 devices
Cleared
Nov 10, 2010
ROSTAM SCENTED AND UNSCENTED BIODEGRADABLE PLASTIC APPLICATOR TAMPONS
Obstetrics & Gynecology
76d
Cleared
May 28, 2009
ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW PLASTIC APPLICATOR TAMPONS
Obstetrics & Gynecology
136d
Cleared
Dec 07, 2006
ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONS
Obstetrics & Gynecology
146d
Cleared
Nov 23, 2004
ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONS
Obstetrics & Gynecology
49d
Cleared
May 28, 2004
PH BUFFERING PLASTIC APPLICATOR TAMPON
Obstetrics & Gynecology
471d
Cleared
Aug 14, 2003
ROSTAM LTD FRAGRANCED PLASTIC APPLICATOR TAMPONS
Obstetrics & Gynecology
38d
Cleared
May 09, 2002
INTERLUDE AND OTHER PRIVATE LABEL PLASTIC APPLICATOR TAMPONS
Obstetrics & Gynecology
79d
Cleared
Aug 03, 2000
TAMPONS
Obstetrics & Gynecology
65d
Cleared
Feb 20, 1997
ROSTAM APPLICATOR TAMPON/ROSTAM NON APPLICATOR TAMPON
Obstetrics & Gynecology
64d