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Cutter Laboratories, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
39
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K861315HYPERBARIC PENETRATION EXTENSION SETMay 21, 1986
K854106BAYSILEXMarch 17, 1986
K842324PERFOURMNovember 9, 1984
K834106INTRAVENOUS INFUSION CONTROLLERMay 30, 1984
K832237ORTHOPEDIC CASTING TAPE MAXCASTAugust 16, 1983
K823214DOSIMETRIC RELEASE PROGRAM - ADMIN. SETJanuary 12, 1983
K821326CUTTER BOND POLYCARBOXYLATE CEMENTMay 28, 1982
K813532CUTTERBOND ZINC PHOSPHATE CEMENTMarch 2, 1982
K802104C-SPLINTSeptember 16, 1980
K802105C-BLADESeptember 16, 1980
K801652TOTAL PARENTERAL NUTRITION SET BAGAugust 27, 1980
K801651CUTTER JETAugust 13, 1980
K800213PHARMACY ADDITIVE SYRINGE SETFebruary 26, 1980
K792250CUTTER POINTSJanuary 23, 1980
K792207PERIDIAL PERITONEAL DIALYSIS TRAYDecember 10, 1979
K790125ULNAR HEAD PROTHESISFebruary 8, 1979
K781937PROTHESIS, METACARPALJanuary 17, 1979
K781521CUTTER RESIFLEX URINE METERNovember 22, 1978
K781668GAMMA RADIATION STERILIZATION PRECEDURENovember 3, 1978
K781059CUTTER/COMPUR MINI CENTRIFUGEAugust 14, 1978