Epiview

FDA 510(k) K961319 · Convatec, A Division of E.R. Squibb & Sons

Substantially Equivalent

510(k) numberK961319

Submission

Device name
Epiview
Applicant
Convatec, A Division of E.R. Squibb & Sons
Skillman, NJ, US
Received
April 5, 1996
Decision date
July 8, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MGP – Dressing, Wound And Burn, Occlusive
Device class
Unclassified

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K001508Laserskin DressingMGP · Traditional Fidia Advanced Biopolymers Srl07/25/2001SE
K990079Fastseal Chest Wound DressingMGP · Traditional Greenfield Medical Technologies, Inc.12/23/1999SE
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K992302Dermaphylyx Skin Protectors, Protect It Skin ProtectorsMGP · Traditional Dermaphylyx, Inc.09/14/1999SE
K992005Giltech Plus Transparent DressingMGP · Traditional Giltech Plus, Inc.09/03/1999SE
K990875Dermaphylyx Film Wound Dressing and Healian Film Wound DressingMGP · Traditional Dermaphylyx, Inc.05/27/1999SN
K990438Dermaflex Wound Dressing, Dermaflex Foam Wound Dressing, Healiaflex Wound Dressing…MGP · Traditional Dermaphylyx, Inc.03/25/1999SE
K984371Mepitel Non Adherent Silicone DressingMGP · Traditional Molnlycke Health Care, Inc.03/03/1999SE

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K013814Absorbent Antimicrobial Wound DressingFRO · Traditional 06/21/2002SE
K990964Signadress Duoderm DressingKGN · Traditional 05/18/1999SE
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K980720Nonwoven PadKMF · Traditional 04/15/1998SE
K980382Non-Woven CompressKMF · Traditional 03/09/1998SN
K974823Nonwoven DressingKMF · Traditional 02/20/1998SN
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Questions and answers

When was Epiview cleared by the FDA?

Epiview (K961319) received a 510(k) decision of Substantially Equivalent on July 8, 1996, 94 days after the submission was received.

What is the product code of K961319?

The FDA product code is MGP – Dressing, Wound And Burn, Occlusive, a Unclassified device.