Ferris Mfg. Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
20
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K031660FERRIS POLYMEM STERILE BREAST PADFebruary 22, 2005
K031307FERRIS POLYMEM SILVER WOUND DRESSINGOctober 22, 2003
K002129FERRIS POLYMEM STERILE WOUND DRESSING WITH COLLAGENAugust 25, 2000
K991729FERRIS POLYOSTOMY STERILE WOUND DRESSINGAugust 27, 1999
K990906FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLERApril 29, 1999
K984539FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSINGMarch 1, 1999
K982306POLYTUBESeptember 22, 1998
K932913FERRIS POLYMEM HYDROPHILIC WOUND DRESSINGJune 7, 1994
K900127FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS)May 18, 1990
K880330FERRIS HYDROPHILIC DRESSINGMarch 23, 1988
K874478DYNAFILMJanuary 14, 1988
K873682FERRIS ECG ELECTRODE W/HYDROGELDecember 29, 1987
K871675FERRIS TRANSPARENT WOUND DRESSING W/HYDROCOLLOIDAugust 6, 1987
K872574TENSAGAINJuly 23, 1987
K865089FERRIS DYNADERM PLUSFebruary 4, 1987
K852375I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVEJuly 11, 1985
K840152FERRIS VENT-A-DERMAugust 30, 1984
K790305ELECTRODES, FERRIS ECG, TYPES 905,906April 3, 1979
K781371BONE MARROW ASPIRATION KITSeptember 20, 1978
K780784ASPIRATION NEEDLEAugust 14, 1978