Bemis Health Care

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K885019BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI.January 25, 1989
K822557SPECIMEN ADAPTOROctober 18, 1982
K822556CRITICAL MEASUREMENT UNITOctober 18, 1982
K803206SUCTION PROBEJanuary 21, 1981
K771737SUCTION CANISTERDecember 20, 1977
K7717338 EMESIS BASINSeptember 28, 1977
K771738MALE URINALSeptember 28, 1977
K760393BED PAN, STACKABLE (AUTOCLAVABLE)August 23, 1976
K760073BASIN, WASH, 6-QT RECTANGULARJuly 20, 1976
K760070TUMBLER, PERSONAL, ROUND, 9 OUNCEJuly 20, 1976
K760072CARAFE, PERSONAL, 1-QT SEMI-RECTANGULARJuly 20, 1976
K760071TRAY, PERSONAL, RECTANG. 8 1/2 X 5 1/4July 20, 1976