Medical Components, Inc. (dba MedComp)
Medical Components, Inc. (dba MedComp) holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2023, with 38 FDA device recalls on record.
Name variants for Medical Components, Inc. (dba MedComp)
as filed with FDA- Medical Components, Inc. (dba MedComp)
- Medical Components, Inc (Dba Medcomp_
Top product codes for Medical Components, Inc. (dba MedComp)
FDA recalls by Medical Components, Inc. (dba MedComp)
10 most recent of 38- Z-1184-2021 — Power Injectable CT Port insertion kits - Product Usage: is an implantable access device designed to provide repeated access to the vascular system.
- Z-2940-2020 — Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Ref: THD155024
- Z-1149-2019 — 14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061422
- Z-2217-2019 — 14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061425 Product Usage: An aid for introducing a hemodialysis catheter
- Z-2216-2019 — 14F x 24CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061424 Product Usage: An aid for introducing a hemodialysis catheter
- Z-2215-2019 — 14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061423 Product Usage: An aid for introducing a hemodialysis catheter
- Z-0222-2020 — C3 Wave App, v. 2.0.5
- Z-2942-2018 — DUO FLOW DOUBLE LUMEN CATHETER, XTP114CT, XTP114MT, ; RAULERSON DUO FLOW IJ DOUBLE LUMEN CATHETER/CATHETER SET, XTP114IJC, XTP114IJS, XTP114IJSE, XTP114MT-C, XTP116IJC, XTP116IJS, XTP116IJSE RAULERSON PRE-CURVED DUO-FLOW IJ DOUBLE LUMEN CATHETER W/SOFT TIP SET, W/MINI SCALPEL, SYRINGE, AND NEEDLE, XTP118IJS-ID; DOUBLE LUMEN CATHETER WITH CURVED EXTENSIONS (CATHETER ONLY), XTP114IJC=, XTP116IJC=, DOUBLE LUMEN IJ CATHETER SET, XTP114IJS=, XTP115IJS=, XTP116IJS=, XTP116IJS=JO, DOUBLE LUMEN CATHETER SET, XTP114MT= DUO-FLOW DOUBLE LUMEN CATHETER, XTP116CT, INTERNAL JUGULAR CATHETER SET, XTP96IJS= (additional product codes/catalog numbers in attached spreadsheet)
- Z-2937-2018 — Duo-Flow XTP Straight Full Set, RMS02105 RMS02108
- Z-2935-2018 — Duo-Flow IJ Full Tray; MCDLT114IJ MCDLT116IJ MCDLT118IJ
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Medical Components, Inc. (dba MedComp)
- K232945 — Trio-CT® Triple Lumen Catheter w/ Curved Extensions
- K202176 — Symetrex LTHD Catheter, Symetrex LTHD Catheter with Sideholes
- K192807 — Duo-Flow Side x Side Double Lumen Catheter
- K183219 — Trio-CT Triple Lumen Catheter
- K181175 — 12F Tri-Flow Triple Lumen Catheter
- K173667 — 15.5F X 19 cm Symetrex Long Term Hemodialysis Catheter with Sideholes, 15.5F X 23 cm Symetrex Long Term Hemodialysis Catheter with Sideholes, 15.5F X 28 cm Symetrex Long Term Hemodialysis Catheter with Sideholes, 15.5F X 33 cm Symetrex Long Term Hemodialysis Catheter with Sideholes, 15.5F X 37 cm Symetrex Long Term Hemodialysis Catheter with Sideholes
- K180567 — C3 Wave System
- K170934 — C3 Wave System
- K170770 — CT Midline
Data sourced from openFDA. This site is unofficial and independent of the FDA.