Medical Device Manufacturer · US , Danville , CA

Euro-Med Intl. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1985
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
1–12 of 16
PROSTATIC CORE-CUT NEEDLE
K883884 · KNW Instrument, Biopsy · Gastroenterology & Urology
Dec 1988 83d
KEVOR-CURETTE
K882404 · PCF Sampler, Endocervical · Obstetrics & Gynecology
Jul 1988 28d
HOOK PROBE
K854890 · KDC Instrument, Surgical, Disposable · General & Plastic Surgery
May 1986 147d
KNIFE
K854891 · EMF Knife, Surgical · General & Plastic Surgery
May 1986 147d
SPOON
K854894 · KDC Instrument, Surgical, Disposable · General & Plastic Surgery
May 1986 147d
BASKET FORCEP
K854895 · KDC Instrument, Surgical, Disposable · General & Plastic Surgery
May 1986 147d
HOOK SCISSOR
K854896 · KDC Instrument, Surgical, Disposable · General & Plastic Surgery
May 1986 147d
MAX-I-GRASP
K854897 · KDC Instrument, Surgical, Disposable · General & Plastic Surgery
May 1986 147d
ATLANTIC GRASPER
K854898 · KDC Instrument, Surgical, Disposable · General & Plastic Surgery
May 1986 147d
PACIFIC GRASPER
K854901 · KDC Instrument, Surgical, Disposable · General & Plastic Surgery
May 1986 147d
FLEX-I-GRASP
K854889 · HRX Arthroscope · Orthopedic
Feb 1986 77d
RANDALL CURETTE
K854888 · FZS Curette, Surgical, General Use · General & Plastic Surgery
Dec 1985 18d
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