FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER— 510(k) K990906

Name: FDA 510(k) clearance K990906
Creator: U.S. Food and Drug Administration
Published: 1999-04-29

Substantially Equivalent for Some Indications

Ferris Mfg. Corp.

FDA 510(k) clearance K990906 for FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER, Substantially Equivalent for Some Indications on 1999-04-29. Applicant: Ferris Mfg. Corp.. Device class: 1.

Clearance details

Applicant: Ferris Mfg. Corp.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1999-03-18
Decision date: 1999-04-29
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Burr Ridge, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KMF

view all

K241916 — TearRepair Liquid Skin Protectant2024-09-27
K182733 — Rochal Bioshield Silicone Film2019-06-27
K171148 — Aleo BME Liquid Bandage2018-01-12
K153571 — Cavilon Advanced High Endurance Skin Protectant2016-08-23
K160684 — Atteris No-Sting Skin Protectant2016-07-26

More clearances from Ferris Mfg. Corp.

view all

K031660 — FERRIS POLYMEM STERILE BREAST PAD2005-02-22
K031307 — FERRIS POLYMEM SILVER WOUND DRESSING2003-10-22
K002129 — FERRIS POLYMEM STERILE WOUND DRESSING WITH COLLAGEN2000-08-25
K991729 — FERRIS POLYOSTOMY STERILE WOUND DRESSING1999-08-27
K984539 — FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSING1999-03-01

Data sourced from openFDA. This site is unofficial and independent of the FDA.