Merit Medical Ireland, Ltd.
FDA 510(k) medical device clearances.
Name variants for Merit Medical Ireland, Ltd.
as filed with FDA- Merit Medical Ireland, Ltd.
- Merit Medical Ireland , Ltd.
Top product codes for Merit Medical Ireland, Ltd.
Recent clearances by Merit Medical Ireland, Ltd.
- K261640 — Merit MAK Nitinol/Gold-Tungsten Guide Wire
- K254137 — InQwire Amplatz Guide Wire
- K253847 — Splashwire Hydrophilic Guide Wire (MSWSTD35150J3)
- K251385 — InQwire Super Stiff Guide Wire (IQSS32180J3); InQwire Super Stiff Guide Wire (IQSS35F260S); InQwire Super Stiff Guide Wire (IQSS35F150S); InQwire Super Stiff Guide Wire (IQSS35F100S); InQwire Super Stiff Guide Wire (IQSS35F80S); InQwire Super Stiff Guide Wire (IQSS35F180S)
- K251181 — Splashwire Hydrophilic Guide Wire (MSWSTD35180J1O5); Splashwire Hydrophilic Guide Wire (MSWSTD35260J1O5); Splashwire Hydrophilic Guide Wire (MSWSTDA35150LT); Splashwire Hydrophilic Guide Wire (MSWSTFA35260LT); Splashwire Hydrophilic Guide Wire (MSWSTFA35150LT); Splashwire Hydrophilic Guide Wire (MSWSTFS38150LT)
- K122321 — BASIXCONPAK ANALOG INFLATION SYRINGE
Data sourced from openFDA. This site is unofficial and independent of the FDA.