Nidacon International AB
Nidacon International AB holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2014.
Top product codes for Nidacon International AB
Recent clearances by Nidacon International AB
- K131145 — PROINSERT
- K092107 — VITRIBLAST, THERMOBLAST, MODEL VB-010, TB-010
- K023206 — SPERM CRYOPROTEC
- K022443 — SPERMASSIST
- K011607 — SPERMCATCH
- K012123 — NIDOIL
- K011606 — PURESPERM BUFFER
- K011346 — READYSWIM
- K002630 — PURESPERM WASH
- K002623 — PURESPERM 40 AND PURESPERM 80
- K984172 — MODIFICATION OF PURESPERM
- K980814 — PURESPERM
Data sourced from openFDA. This site is unofficial and independent of the FDA.