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Latex Ind., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K812058AKRON URINARY DRAINAGE BATJuly 31, 1981
K810281UROLOGICAL CATHETERSFebruary 25, 1981
K791674BLADDER RETENTION CATHETERIZATION TRAYNovember 5, 1979
K781751CATHETER, AKRON FOLEY TEFLONJanuary 22, 1979
K781433AKRON MALE EXTERNAL CATHETERNovember 3, 1978
K772277BLADDER RETENTION-CATHETHERIZATIONTRAYMarch 2, 1978
K772340CATHETERIZATION KIT 732016-732018February 24, 1978
K772342ROBINSON KIT - 750014 & 750016February 24, 1978
K772341BLADDER KIT - 734000February 24, 1978
K780268BLADDER CATH KIT W/OUT CATHETERFebruary 24, 1978
K780267CATH TRAY W/OUT CATHETERFebruary 24, 1978
K771650AKRO-SIL FOLEY KIT 30CCSeptember 20, 1977
K771651AKRO-SIL FOLEY KIT 5CCSeptember 20, 1977
K771652CATH-CARE TRAYSeptember 20, 1977