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Sybron Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
37
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K862284SEALITEJune 23, 1986
K854855PROOF ALGINATE IMPRESSION MATERIALJanuary 30, 1986
K844092DIAGNOSTIC MICROSOPCE SLIDESOctober 25, 1984
K842132TYCOS SELF-CHECK/DIGITAL FEVER THERMOJuly 18, 1984
K841910KERR SEALAPEX ROOT CANAL SEALERJuly 13, 1984
K841732LIEBEL-FLARSHEIM AFC 1000 X-RAY FILMJune 5, 1984
K840469TYCOS SELF CHECK BPM3 BLOOD PRESS MONIMay 21, 1984
K840407KERR RESIN BONDED BRIDGE CEMENTMay 21, 1984
K840607LF MOTORIZED RADIOGRAPHIC FILM VIEWERMarch 5, 1984
K833138DIGITAL INJECTOR SYSNovember 14, 1983
K823795EVERBOND GLASS IONOMER CEMENTJanuary 26, 1983
K822869COMMAND BONDING RESIN/GLAZE/OPAQUEROctober 13, 1982
K820681CASTLE(R) 2510 & 2610 MINOR SURG. LIGHTApril 15, 1982
K820783CASTLE MICROCOMPUTER STERILIZER CONTROLApril 15, 1982
K820494SYBRON BOVIE CSV HAND CONTR. ELECTROSURGApril 9, 1982
K820182SYBRON/KERR COMMANDMarch 2, 1982
K820135TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETERMarch 1, 1982
K820183SYBRON/KERR MIRROR 3February 24, 1982
K820181SYBRON/KERR CONTOURFebruary 24, 1982
K813201CASTLE #3241 GAS AERATORDecember 31, 1981