Conception Technologies is one of 25845 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Conception Technologies - FDA 510(k) Cleared Devices
Recent clearances: ENHANCE HUMAN SERUM ALBUMIN, ENHANCE HTF MEDIUM WITH HEPES, SPERM WASH MEDIUM WITH GENTAMICIN
8
Total
8
Cleared
0
Denied
Conception Technologies has 8 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 8 cleared submissions from 2000 to 2003. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Conception Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Conception Technologies
8 devices
Cleared
Apr 08, 2003
ENHANCE HUMAN SERUM ALBUMIN
Obstetrics & Gynecology
22d
Cleared
Dec 13, 2002
ENHANCE HTF MEDIUM WITH HEPES
Obstetrics & Gynecology
44d
Cleared
Dec 13, 2002
SPERM WASH MEDIUM WITH GENTAMICIN
Obstetrics & Gynecology
38d
Cleared
Mar 28, 2002
PBS, PBSW WITH CATIONS AND PHENOL RED
Obstetrics & Gynecology
43d
Cleared
Jul 02, 2001
10% PVP
Obstetrics & Gynecology
49d
Cleared
Jul 02, 2001
HYALURONIDASE IN HTF MEDIUM
Obstetrics & Gynecology
42d
Cleared
Jun 13, 2001
OIL FOR TISSUE CULTURE
Obstetrics & Gynecology
30d
Cleared
Aug 02, 2000
WATER FOR TISSUE CULTURE, MODELS 1500
Obstetrics & Gynecology
317d