Ocean Medical Products, Ltd. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Ocean Medical Products, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1981 to 1988. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ocean Medical Products, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ocean Medical Products, Ltd.
9 devices
Cleared
Jun 15, 1988
SOFT TISSUE BIOPSY DEVICE
General & Plastic Surgery
33d
Cleared
Mar 18, 1987
NOTCH-NEEDLE, WESCOTT STYLE
General & Plastic Surgery
13d
Cleared
Oct 18, 1984
SINGLE WALL INTRODUCER NEEDLE
Cardiovascular
24d
Cleared
Feb 07, 1983
MYELOGRAPHY NEEDLE
General Hospital
61d
Cleared
Jan 07, 1983
SPINAL NEEDLE
Anesthesiology
30d
Cleared
Mar 01, 1982
MADAYAG TYPE NEEDLE
Gastroenterology & Urology
80d
Cleared
Jan 07, 1982
POTTS-COURNAND STYLE NEEDLE
General & Plastic Surgery
27d
Cleared
Jan 07, 1982
CHIBA SKINNY NEEDLE
General & Plastic Surgery
27d
Cleared
Dec 29, 1981
PERCUTANEOUS ENTRY NEEDLE, SELDINGER
Cardiovascular
18d