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Cadwell Laboratories, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
46
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K061706CADWELL EASYNET OXIMETER MODULEMarch 5, 2007
K061705CADWELL EASYNET NASAL PRESSURE MODULENovember 21, 2006
K042350TES-1 CONSTANT VOLTAGE ELECTRICAL STIMULATORNovember 3, 2004
K040986CADWELL LIMB MOVEMENT MODULEJuly 1, 2004
K040932EASYNET BODY POSITION MODULEJuly 1, 2004
K971214KILOWINJune 11, 1998
K962457TWO-CHANNEL PREAMPLIFIERJanuary 13, 1997
K962455FOUR-CHANNEL PREAMPLIFIERJanuary 13, 1997
K962458CADWELL FOUR-/EIGHT-CHANNEL PREAMPLIFIERJanuary 13, 1997
K946094CADWELL EASY AMBULATORY EEGSeptember 12, 1995
K933808EEG CUP ELECTRODEDecember 29, 1994
K933796EEG NEEDLE ELECTRODEDecember 29, 1994
K933805RING ELECTRODEDecember 19, 1994
K933801ELECTRODE, CUTANEOUSOctober 21, 1994
K933802CUTANEOUS ELECTRODESeptember 7, 1994
K933807GROUND PLATE ELECTRODEJuly 26, 1994
K933803DISPOSABLE TAB ELECTRODEJuly 8, 1994
K933799TEN-20 CONDUCTIVE PASTE GELMay 27, 1994
K933797OMNI PREP GELMay 17, 1994
K933798NU-PREP GELApril 22, 1994