Randwal Instrument Co., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K873990IRAS EDS INTERFEROMETRIC STIMULATORFebruary 5, 1988
K873987IRAS GLARE TESTERNovember 24, 1987
K864012IRAS PERIMETERDecember 12, 1986
K853556LASER IRASNovember 1, 1985
K842567PORTABLE ACUIOMETERAugust 15, 1984
K827577VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETERJanuary 24, 1983