Ferris Mfg. Corp.
Ferris Mfg. Corp. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 2005.
Top product codes for Ferris Mfg. Corp.
Recent clearances by Ferris Mfg. Corp.
- K031660 — FERRIS POLYMEM STERILE BREAST PAD
- K031307 — FERRIS POLYMEM SILVER WOUND DRESSING
- K002129 — FERRIS POLYMEM STERILE WOUND DRESSING WITH COLLAGEN
- K991729 — FERRIS POLYOSTOMY STERILE WOUND DRESSING
- K990906 — FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER
- K984539 — FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSING
- K982306 — POLYTUBE
- K932913 — FERRIS POLYMEM HYDROPHILIC WOUND DRESSING
- K900127 — FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS)
- K880330 — FERRIS HYDROPHILIC DRESSING
- K874478 — DYNAFILM
- K873682 — FERRIS ECG ELECTRODE W/HYDROGEL
- K871675 — FERRIS TRANSPARENT WOUND DRESSING W/HYDROCOLLOID
- K872574 — TENSAGAIN
- K865089 — FERRIS DYNADERM PLUS
- K852375 — I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVE
- K840152 — FERRIS VENT-A-DERM
- K790305 — ELECTRODES, FERRIS ECG, TYPES 905,906
- K781371 — BONE MARROW ASPIRATION KIT
- K780784 — ASPIRATION NEEDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.