Invitrocare, Inc. is one of 25849 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Invitrocare, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ISOCARE ONE STEP SPERM PROCESSING MEDIUM CAT# 2207-12, HYALURONIDASE REAGENT, MODEL CAT#2212, PVP-POLYVINYLPYRROLIDONE REAGENT, MODEL CAT#2210
10
Total
10
Cleared
0
Denied
Invitrocare, Inc. has 10 FDA 510(k) cleared obstetrics & gynecology devices. Based in San Diego, US.
Historical record: 10 cleared submissions from 2000 to 2002.
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 - Invitrocare, Inc.
10 devices
Cleared
Dec 26, 2002
ISOCARE ONE STEP SPERM PROCESSING MEDIUM CAT# 2207-12
Obstetrics & Gynecology
90d
Cleared
Jan 17, 2001
HYALURONIDASE REAGENT, MODEL CAT#2212
Obstetrics & Gynecology
43d
Cleared
Aug 14, 2000
PVP-POLYVINYLPYRROLIDONE REAGENT, MODEL CAT#2210
Obstetrics & Gynecology
47d
Cleared
Jun 13, 2000
IVC THREE BLASTOCYST MEDIUM, CAT # 2007
Obstetrics & Gynecology
68d
Cleared
Jun 08, 2000
SPERM WASH MEDIUM, CAT# 2003/2005
Obstetrics & Gynecology
72d
Cleared
May 25, 2000
IVC TWO MEDIUM
Obstetrics & Gynecology
63d
Cleared
May 25, 2000
IVC ONE MEDIUM
Obstetrics & Gynecology
63d
Cleared
May 25, 2000
Q-HTF, CAT# 2001
Obstetrics & Gynecology
224d
Cleared
May 04, 2000
HTF-HEPES
Obstetrics & Gynecology
42d
Cleared
May 04, 2000
HUMAN SERUM ALBUMIN (HSA)
Obstetrics & Gynecology
42d