Kelleher Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
94
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K822618EMERGENCY TRACHEOSTOMY INSTRUMENT SETJanuary 28, 1983
K822268NAGASHIMA NS-III ELECTRONYSTAGMOGRAPHJanuary 28, 1983
K823083ELECTROSURGICAL UNITDecember 7, 1982
K823111NYSTYMOGRAPH ACCESSNovember 22, 1982
K822252ENT TREATMENT UNITSNovember 22, 1982
K822272HEAD MIRRORS W/HEAD LAMPS & HEAD BANDSNovember 10, 1982
K822017TYMPANOSTOMY TUBES & VARIOUS TYPESOctober 27, 1982
K822257VARIOUS TYPES OF LIGHT SOURCE HANDLESOctober 26, 1982
K822259LARYNGEAL SPATULASOctober 22, 1982
K822004FACE SHIELDSOctober 20, 1982
K822185LARYNGEAL SYRINGEOctober 18, 1982
K822267TRANSFORMEROctober 13, 1982
K822264NAGASHIMA SN OPERATOR'S CHAIROctober 13, 1982
K822201EAR CANNULASOctober 6, 1982
K822569TYMPANOPLASTY & SKIN DISSECTORSOctober 6, 1982
K822265FIBEROPTIC LIGHT SOURCE W/RELATED ITEMSSeptember 28, 1982
K822179FRENZEL EYEGLASSES & RELATED ITEMSSeptember 21, 1982
K822204ENT MALLETSSeptember 17, 1982
K822568EAR PROBESSeptember 14, 1982
K822566AURAL REFLEX INDICATORSeptember 14, 1982