FDA applicant
Med Telectronics, Ltd.
FDA records 5 decisions for Med Telectronics, Ltd. (Mchenry, IL) in 1977: 5 510(k) clearances. Most are in product codes DTB (Permanent Pacemaker Electrode) and DXY (Implantable Pacemaker Pulse-Generator). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Med Telectronics, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Med Telectronics, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Med Telectronics, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report