Humagen Fertility Diagnostics, Inc. is one of 9103 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Humagen Fertility Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INTRACYTOPLASMIC SPERM INJECTION MICROPIPETS (ICSI) SPERMATID ICSI MICROPIPETS, HOLDING MICROPIPETS, ASSISTED HATCHING M, NEWLIFE DISH (ETCHED OR NON-ETCHED, WITH OR WITHOUT LID), MODELS 14-52, 1452E, 1452EL, 1452L
5
Total
5
Cleared
0
Denied
Humagen Fertility Diagnostics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Charlottesville, US.
Historical record: 5 cleared submissions from 1994 to 2002. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Humagen Fertility Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Humagen Fertility Diagnostics, Inc.
5 devices
Cleared
Feb 11, 2002
BLASTOMERE BIOPSY MICROPIPET, POLAR BODY MICROPIPET, MODELS...
Obstetrics & Gynecology
173d
Cleared
May 12, 2000
PASTEUR PIPET - STERILE 9, PASTEUR PIPET - STERILE 5 3/4, MODELS 16-PP-9,...
Obstetrics & Gynecology
51d
Cleared
Jul 14, 1999
INTRACYTOPLASMIC SPERM INJECTION MICROPIPETS (ICSI) SPERMATID ICSI...
Obstetrics & Gynecology
121d
Cleared
Jul 14, 1999
NEWLIFE DISH (ETCHED OR NON-ETCHED, WITH OR WITHOUT LID), MODELS 14-52,...
Obstetrics & Gynecology
114d
Cleared
Aug 30, 1994
SEMEN ANALYSIS KIT
Hematology
1014d