Home / Companies / Midwest X-Ray Equipment Co.

Midwest X-Ray Equipment Co.

FDA Regulatory Profile

Midwest X-Ray Equipment Co. 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 January 15, 1993.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K924423MWX-7440 HIGH SPEED BUCKYJanuary 15, 1993
K827609MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAYJuly 9, 1982
K827504SIZE SENSING CASSETTE TRAYJune 9, 1982

FDA data resources