Kitazato IUI Catheter— 510(k) K162667
Substantially EquivalentKitazato Corporation
FDA 510(k) clearance K162667 for Kitazato IUI Catheter, Substantially Equivalent on 2017-05-11. Applicant: Kitazato Corporation. Device class: 2.
Clearance details
- Applicant
- Kitazato Corporation
- Product code
- Code MQF
- Device class
- Class 2
- Regulation
- 21 CFR 884.6110
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tokyo, JP
Recent devices under product code MQF
view all- K253354 — Minvitro Embryo Transfer Catheters (ETCA23175, ETCA23175-C, ETCB20175, ETCB20175-C, ETCB20175-ET, ETCB20175-ET-C)
- K243373 — Embryo Transfer Catheter (ETC) Assortment: EmbryoCath Embryo Transfer Catheter - Pre-curved 230 mm (REF 17500) +4 more
- K240307 — VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)
- K231730 — FemaSeed Intratubal Insemination
- K220010 — Daylily Single Use Sterile Embryo Transfer Catheter
More clearances from Kitazato Corporation
view all- K260248 — Ultra-Fast Warm
- K251305 — Ultra-Fast Vitri; Ultra-Fast Warm
- K200249 — Sequential Culture Media (Fertilization Medium [without HSA/rHA, with HSA, with rHA], Cleavage Medium [without HSA/rHA, with HSA, with rHA], Blastocyst Medium [without HSA/rHA, with HSA, with rHA])
- K193522 — iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA
- K192845 — Sperm Freeze, Sperm Fridge
Data sourced from openFDA. This site is unofficial and independent of the FDA.