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Ocean Medical Products, Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K882013SOFT TISSUE BIOPSY DEVICEJune 15, 1988
K870896NOTCH-NEEDLE, WESCOTT STYLEMarch 18, 1987
K843719SINGLE WALL INTRODUCER NEEDLEOctober 18, 1984
K823693MYELOGRAPHY NEEDLEFebruary 7, 1983
K823692SPINAL NEEDLEJanuary 7, 1983
K813462MADAYAG TYPE NEEDLEMarch 1, 1982
K813460CHIBA SKINNY NEEDLEJanuary 7, 1982
K813448POTTS-COURNAND STYLE NEEDLEJanuary 7, 1982
K813461PERCUTANEOUS ENTRY NEEDLE, SELDINGERDecember 29, 1981