Medicult A/S is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medicult A/S - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
Medicult A/S has 26 FDA 510(k) cleared obstetrics & gynecology devices. Based in San Diego, US.
Historical record: 26 cleared submissions from 2000 to 2008.
Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medicult A/S
26 devices
Cleared
Dec 18, 2008
BLASTASSIST WITHOUT PHENOL RED, MODEL REF 1215, BLASTASSIST WITH PHENOL RED,...
Obstetrics & Gynecology
329d
Cleared
Sep 19, 2008
ICSI CUMULASE
Obstetrics & Gynecology
100d
Cleared
Sep 03, 2008
EMBRYOASSIST AND EMBRYOASSIST WITH PHENOL RED
Obstetrics & Gynecology
195d
Cleared
Feb 08, 2007
EMBRYOASSIST
Obstetrics & Gynecology
274d
Cleared
Oct 02, 2006
SPERMSLOW
Obstetrics & Gynecology
160d
Cleared
Jul 28, 2006
BIOPSY MEDIUM, MODEL REF 1062
Obstetrics & Gynecology
109d
Cleared
May 10, 2006
SYNVITRO CUMULASE (HYALURONIDASE MEDIUM)
Obstetrics & Gynecology
55d
Cleared
Nov 22, 2004
MEDICULT IVM SYSTEM
Obstetrics & Gynecology
193d
Cleared
Aug 20, 2003
ISM1+, IMS2+, AND UTM+
Obstetrics & Gynecology
187d
Cleared
Jun 27, 2003
BLASTFREEZE AND BLASTTHAW
Obstetrics & Gynecology
46d
Cleared
Jun 24, 2003
SYNVITRO HYADASE
Obstetrics & Gynecology
67d
Cleared
Mar 22, 2001
BLASTASSIST SYSTEM
Obstetrics & Gynecology
163d