Cavi-Care Conforming Foam Dressing

FDA 510(k) K943619 · Smith & Nephew United, Inc.

Substantially Equivalent for Some Indications

510(k) numberK943619

Submission

Device name
Cavi-Care Conforming Foam Dressing
Applicant
Smith & Nephew United, Inc.
Largo, FL, US
Received
July 27, 1994
Decision date
August 19, 1994
Decision
Substantially Equivalent for Some Indications (SN)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KMF – Bandage, Liquid
Device class
Class I (low risk)
Regulation
21 CFR 880.5090
Specialty
General Hospital

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More from Polichem S.A

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K963096Allevyn Hydro Poly Dressing ND All Trac DressingKMF · Traditional 10/25/1996SE
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K945330Allevyn AdhesiveKMF · Traditional 02/09/1995SN
K942748IntrasiteNAE · Traditional 06/29/1994SN
K935705Allevyn Island Wound DressingNAE · Traditional 02/15/1994SE
K935803Cica-Care Silicone Gel SheetMDA · Traditional 02/03/1994SE
K932263Solosite Dermal Wound GelMGQ · Traditional 10/01/1993SE
K926508Intrasite GelNAE · Traditional 07/13/1993SE
K922897StrappalKGX · Traditional 09/15/1992SE
K914147Allevlyn Wound Dressing, ModificationKMF · Traditional 02/03/1992SE

Questions and answers

When was Cavi-Care Conforming Foam Dressing cleared by the FDA?

Cavi-Care Conforming Foam Dressing (K943619) received a 510(k) decision of Substantially Equivalent for Some Indications on August 19, 1994, 23 days after the submission was received.

What is the product code of K943619?

The FDA product code is KMF – Bandage, Liquid, a Class I (low risk) device regulated under 21 CFR 880.5090.