Site Strip

FDA 510(k) K843200 · E-Med Corp.

Substantially Equivalent

510(k) numberK843200

Submission

Device name
Site Strip
Applicant
E-Med Corp.
Cincinnati, OH, US
Received
August 14, 1984
Decision date
March 12, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
NAD – Dressing, Wound, Occlusive
Device class
Class I (low risk)
Regulation
21 CFR 878.4020
Specialty
General, Plastic Surgery

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K254246LT Antibacterial Foam with Silver DressingNAD · Traditional Zhejiang Longterm Medical Technology Co., Ltd.09/10/2026SE
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K091133Aplion Topical Care SystemNAD · Traditional Aplion Medical,Llc05/20/2009SE
K072560Envela (Hydrohesive Occlusive Dressing)NAD · Traditional Teikoku Pharma USA, Inc.06/17/2008SE
K080524Centurion Sorbaview OTCNAD · Traditional Tri-State Hospital Supply Corp.04/23/2008SE
K060046DermastreamNAD · Traditional Enzysurge , Ltd.02/27/2006SE
K043063Oxyband Wound DressingNAD · Traditional Oxyband Technologies, Inc.03/24/2005SE
K020781Wet ChamberNAD · Traditional Kinetic Concepts, Inc.05/06/2002SE
K990530Kerlix MD Antimicrobial Gauze DressingNAD · Traditional The Kendall Company, L.P.01/31/2000SE
K990861Wound Dressing/Abd Pad, Model #10810NAD · Traditional Hospital Specialty Co.04/12/1999SE

More from Hospital Specialty Co.

510(k)DeviceDecision
K971619Microfuse Membrane Infusion CatheterKRA · Traditional 02/27/1998SE
K792049I.V. StripKMK · Traditional 11/20/1979SE

Questions and answers

When was Site Strip cleared by the FDA?

Site Strip (K843200) received a 510(k) decision of Substantially Equivalent on March 12, 1985, 210 days after the submission was received.

What is the product code of K843200?

The FDA product code is NAD – Dressing, Wound, Occlusive, a Class I (low risk) device regulated under 21 CFR 878.4020.