Medelec Intl. Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medelec Intl. Corp. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Medelec Intl. Corp. has 15 FDA 510(k) cleared medical devices. Based in Miami Beach, US.
Historical record: 15 cleared submissions from 1985 to 1996.
Browse the FDA 510(k) cleared devices submitted by Medelec Intl. Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medelec Intl. Corp.
15 devices
Cleared
Dec 20, 1996
DISPOSABLE NEEDLE ELECTRODE
Neurology
282d
Cleared
Jul 28, 1994
TD50 ELECTROMYOGRAPH
Neurology
282d
Cleared
Nov 03, 1992
MEDELEC 2110 AND 2114 EEG
Neurology
155d
Cleared
Jun 10, 1992
ELECTROENCEPHALOGRAPH RECORDING SYSTEM
Neurology
152d
Cleared
Nov 08, 1991
SAPPHIRE 4ME EMG/EP SYSTEM
Neurology
137d
Cleared
May 20, 1987
PROPHYLACTIC (CONDOM) MR. JOHNNY
Obstetrics & Gynecology
140d
Cleared
Oct 24, 1986
BLOOD SPECIMEN COLLECTION DEVICES
Chemistry
46d
Cleared
Apr 11, 1986
PROPHYLACTIC (CONDOM)
Obstetrics & Gynecology
144d
Cleared
Jan 09, 1986
CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I
General Hospital
56d
Cleared
Dec 24, 1985
SCALPEL, ONE-PIECE, DISPOSABLE
General & Plastic Surgery
19d
Cleared
Dec 24, 1985
SCALPEL HANDLE
General & Plastic Surgery
19d
Cleared
Dec 24, 1985
BLADES, SCALPEL STAINLESS STEEL
General & Plastic Surgery
19d
Cleared
Dec 24, 1985
BLADES, SCALPEL CARBON STEET
General & Plastic Surgery
19d
Cleared
Dec 09, 1985
DISPOSABLE SYRINGES & NEEDLES
General Hospital
25d
Cleared
Dec 02, 1985
BLADE, SCALPEL
General & Plastic Surgery
18d