CURADERM ALGINATE HYDROCOLLOID— 510(k) K943636

Name: FDA 510(k) clearance K943636
Creator: U.S. Food and Drug Administration
Published: 1994-10-03

Substantially Equivalent for Some Indications

Kendall Healthcare Products Co. Div.Of Tyco Health

FDA 510(k) clearance K943636 for CURADERM ALGINATE HYDROCOLLOID, Substantially Equivalent for Some Indications on 1994-10-03. Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health. Device class: 1.

Clearance details

Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1994-07-27
Decision date: 1994-10-03
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Mansfield, MA, 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 Kendall Healthcare Products Co. Div.Of Tyco Health

view all

K973763 — KENDALL CURITY IODOFORM PACKING STRIP1997-12-31
K973511 — KENDALL CURITY PETROLATUM GAUZE1997-12-16
K973507 — KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)1997-12-15
K973619 — KENDALL CURITY NON-ADHERING DRESSING1997-12-10
K973509 — KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING1997-12-04

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