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Dutchland Laboratories, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
75
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K821912MCCOY'S POWDER MEDIUM 5A SUSPENSIONJuly 27, 1982
K821919POWDERED RPMI-1634 MEDIUMJuly 27, 1982
K821918POWDERED RPMI-1603 MEDIUMJuly 27, 1982
K821911S-MEM-JOKLIK'S POWDERJuly 27, 1982
K821917WAYMOUTH'S POWDER MEDIUMJuly 27, 1982
K821913ISCOVE'S MODIFIED DULBECCO POWDER MEDIUMJuly 27, 1982
K821914COON'S F-12 POWDER MEDIUMJuly 27, 1982
K821916IMPROVED MEM-RICHTER'S POWDER MODIF.July 27, 1982
K821915BME AUTOCLAVABLE MEDIUMJuly 27, 1982
K820925H - BME POWDERED MEDIUMApril 21, 1982
K820914EMEM POWERED MEDIUMApril 21, 1982
K820927HBS POWDERApril 21, 1982
K820923DULBECCO'S PBS POWDERApril 21, 1982
K820930FISCHER'S POWDERED MEDIUMApril 21, 1982
K820917L-15 POWDERED MEDIUMApril 21, 1982
K820931HANK'S 199 POWDERED MEDIUMApril 21, 1982
K820915MEM AUTOCLAVABLE MEDIUMApril 21, 1982
K820916D-MEM-HIGH GLUCOSE-POWDERED MEDIUMApril 21, 1982
K820920MCCOY'S 5A POWDERED MEDIUMApril 21, 1982
K820924HAMS F-12 POWDERED MEDIUMApril 21, 1982