Euro-Med Intl. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Euro-Med Intl. has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Danville, US.
Historical record: 16 cleared submissions from 1985 to 1988.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
16 devices
Cleared
Dec 05, 1988
PROSTATIC CORE-CUT NEEDLE
Gastroenterology & Urology
83d
Cleared
Jul 08, 1988
KEVOR-CURETTE
Obstetrics & Gynecology
28d
Cleared
May 02, 1986
HOOK PROBE
General & Plastic Surgery
147d
Cleared
May 02, 1986
KNIFE
General & Plastic Surgery
147d
Cleared
May 02, 1986
SPOON
General & Plastic Surgery
147d
Cleared
May 02, 1986
BASKET FORCEP
General & Plastic Surgery
147d
Cleared
May 02, 1986
HOOK SCISSOR
General & Plastic Surgery
147d
Cleared
May 02, 1986
MAX-I-GRASP
General & Plastic Surgery
147d
Cleared
May 02, 1986
ATLANTIC GRASPER
General & Plastic Surgery
147d
Cleared
May 02, 1986
PACIFIC GRASPER
General & Plastic Surgery
147d
Cleared
Feb 21, 1986
FLEX-I-GRASP
Orthopedic
77d
Cleared
Dec 24, 1985
RANDALL CURETTE
General & Plastic Surgery
18d
Cleared
Dec 24, 1985
RULER
General & Plastic Surgery
18d
Cleared
Dec 24, 1985
KEYES SKIN PUNCH
General & Plastic Surgery
18d
Cleared
Dec 24, 1985
NOVAK CURETTE
General & Plastic Surgery
18d
Cleared
Dec 24, 1985
EPISIOTOMY SCISSORS
General & Plastic Surgery
18d