RYNEL MEDICAL FOAM— 510(k) K951909

Substantially Equivalent

Rynel, Ltd. Inc.

FDA 510(k) clearance K951909 for RYNEL MEDICAL FOAM, Substantially Equivalent on 1995-06-21. Applicant: Rynel, Ltd. Inc.. Device class: 1.

Clearance details

Applicant: Rynel, Ltd. Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1995-04-24
Decision date: 1995-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boothbay, ME, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KMF

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 Rynel, Ltd. Inc.

K971337 — EPITECH ISLAND DRESSINGS1997-07-09

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