Medical Device Manufacturer · US , Charlottesville , VA

Humagen Fertility Diagnostics, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1994

Recent clearances: BLASTOMERE BIOPSY MICROPIPET, POLAR BODY MICROPIPET, MODELS 10-MBB,10-MBB-B,10-MPB,10-MPB-B, PASTEUR PIPET - STERILE 9, PASTEUR PIPET - STERILE 5 3/4, MODELS 16-PP-9, 16-PP-5.75, INTRACYTOPLASMIC SPERM INJECTION MICROPIPETS (ICSI) SPERMATID ICSI MICROPIPETS, HOLDING MICROPIPETS, ASSISTED HATCHING M

View 5 510(k) Devices ↓

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.

Humagen Fertility Diagnostics, Inc. is one of 23726 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Humagen Fertility Diagnostics, Inc.

5 devices

1-5 of 5

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