Medelec Intl. Corp.
Medelec Intl. Corp. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1996.
Top product codes for Medelec Intl. Corp.
Recent clearances by Medelec Intl. Corp.
- K961013 — DISPOSABLE NEEDLE ELECTRODE
- K935017 — TD50 ELECTROMYOGRAPH
- K922548 — MEDELEC 2110 AND 2114 EEG
- K920127 — ELECTROENCEPHALOGRAPH RECORDING SYSTEM
- K912775 — SAPPHIRE 4ME EMG/EP SYSTEM
- K865106 — PROPHYLACTIC (CONDOM) MR. JOHNNY
- K863491 — BLOOD SPECIMEN COLLECTION DEVICES
- K854622 — PROPHYLACTIC (CONDOM)
- K854562 — CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I
- K854857 — SCALPEL, ONE-PIECE, DISPOSABLE
- K854858 — SCALPEL HANDLE
- K854859 — BLADES, SCALPEL STAINLESS STEEL
- K854860 — BLADES, SCALPEL CARBON STEET
- K854563 — DISPOSABLE SYRINGES & NEEDLES
- K854561 — BLADE, SCALPEL
Data sourced from openFDA. This site is unofficial and independent of the FDA.