Rovers Diagnostic Devices

FDA Regulatory Profile

Rovers Diagnostic Devices appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 28, 1995.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K941472CERVEX-BRUSH PAP KITFebruary 28, 1995
K942843CERVEX-BRUSH(R), STERILE, SPATULA, CERVICAL, CYTOLOGYDecember 8, 1994
K942144URETHRA-BRUSHJune 27, 1994