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Cameron-Miller, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K944775ELECTROSURGICAL UNIT MODEL 26-0335October 11, 1994
K931541MODEL 26-0375, ELECTROSURGICAL GENERATORJune 1, 1994
K931437MODEL 80-1983, ELECTROSURGICAL GENERATORMay 27, 1994
K935490ELECTROSURGICAL DEVICE, MODEL 26-2500April 1, 1994
K853972CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATORJanuary 24, 1986
K854109ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345January 24, 1986
K833449HAND CONTROLLED PENCIL OR SWITCH HANDNovember 29, 1983
K822092CAMERON-MILLER #40-1516September 21, 1982
K812702TECHNICATORNovember 5, 1981
K791415MODEL 80-1765 ELECTROSURGICAL UNITOctober 11, 1979
K781353PAPILLOTOME CUTTING SNAREOctober 10, 1978
K780433FIBER OPTIC ADJUSTABLE HEADLIGHTJune 13, 1978
K772235HAND CONTROL ACCESS.-ELECTROSURG. UNITSDecember 13, 1977
K771639ELECTROSURGICAL GENERATORNovember 29, 1977