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Lake Medical Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K943162LAKE STAGEZERO(TM) AIR FLOTATION BEDFebruary 27, 1995
K922730LAKE OSTOMY CARE SETDecember 30, 1993
K905053STAGE ZERO AIR FLOTATION BEDNovember 26, 1990
K901835LAKE N/G FEEDING TUBE (WITH Y PORT CONNECTOR)September 5, 1990
K902508LAKE MALE EXTERNAL CATHETERIZATION KITAugust 23, 1990
K902121LAKE GASTROSTOMY TUBEJuly 27, 1990
K884127LAKE N/G FEEDING TUBEFebruary 8, 1989
K884128LAKE N/G EXTENSION SETDecember 8, 1988
K883610LAKE FOLEY CATHETERIZATION TRAYOctober 12, 1988
K880578LAKE DISPOSABLE PROBE COVERMarch 31, 1988
K875383LAKE CATHETER CARE KITS (MODIFICATION)March 9, 1988
K873991LAKE IRRIGATION TRAYDecember 30, 1987
K873973LAKE WOUND CARE/TREATMENT KITNovember 20, 1987
K872750LAKE CATHETER CARE KITSeptember 3, 1987
K872244CORD-ASSURE UMBILICAL BLOOD GAS KITJuly 21, 1987