Advanced Reproductive Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Reproductive Technologies - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Advanced Reproductive Technologies has 5 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 5 cleared submissions from 2000 to 2000. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Advanced Reproductive Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Advanced Reproductive Technologies
5 devices
Cleared
Apr 19, 2000
OIL FOR TISSUE CULTURE
Obstetrics & Gynecology
364d
Cleared
Feb 15, 2000
QUINN'S HTF MEDIUM, QUINN'S HTF MEDIUM WITH HEPES, QUINN'S BASAL XI HTF...
Obstetrics & Gynecology
300d
Cleared
Feb 07, 2000
HUMAN SERUM ALBUMIN
Obstetrics & Gynecology
292d
Cleared
Feb 02, 2000
QUINN'S SPERM WASHING MEDIUM
Obstetrics & Gynecology
287d
Cleared
Jan 10, 2000
PVP, POLYVINYLPYRROLIDONE 10% (W/V) IN HEPES-HTF
Obstetrics & Gynecology
264d