Randwal Instrument Co., Inc.

FDA Regulatory Profile

Randwal Instrument Co., Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 5, 1988.

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