Conception Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Conception Technology, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Conception Technology, Inc. has 5 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 5 cleared submissions from 1998 to 2003. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Conception Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Conception Technology, Inc.
5 devices
Cleared
Mar 20, 2003
ENHANCE SPERM FREEZE
Obstetrics & Gynecology
66d
Cleared
Feb 12, 2003
ENHANCE-S PLUS H
Obstetrics & Gynecology
30d
Cleared
Jul 26, 1999
ENHANCE-S PLUS
Obstetrics & Gynecology
98d
Cleared
Jul 19, 1999
MICROTOOLS
Obstetrics & Gynecology
109d
Cleared
Jan 07, 1998
OVULON MONITOR
Toxicology
90d