Humagen Fertility Diagnostics, Inc.
Humagen Fertility Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2002.
Top product codes for Humagen Fertility Diagnostics, Inc.
Recent clearances by Humagen Fertility Diagnostics, Inc.
- K012811 — BLASTOMERE BIOPSY MICROPIPET, POLAR BODY MICROPIPET, MODELS 10-MBB,10-MBB-B,10-MPB,10-MPB-B
- K000915 — PASTEUR PIPET - STERILE 9, PASTEUR PIPET - STERILE 5 3/4, MODELS 16-PP-9, 16-PP-5.75
- K990847 — INTRACYTOPLASMIC SPERM INJECTION MICROPIPETS (ICSI) SPERMATID ICSI MICROPIPETS, HOLDING MICROPIPETS, ASSISTED HATCHING M
- K990941 — NEWLIFE DISH (ETCHED OR NON-ETCHED, WITH OR WITHOUT LID), MODELS 14-52, 1452E, 1452EL, 1452L
- K915229 — SEMEN ANALYSIS KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.