Aegis Non-Adherent Dressing

FDA 510(k) K820413 · Professional Medical Products, Inc.

Substantially Equivalent

510(k) numberK820413

Submission

Device name
Aegis Non-Adherent Dressing
Applicant
Professional Medical Products, Inc.
Mchenry, IL, US
Received
February 12, 1982
Decision date
March 12, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
NAB – Gauze / Sponge,Nonresorbable For External Use
Device class
Class I (low risk)
Regulation
21 CFR 878.4014
Specialty
General, Plastic Surgery

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K925590Multi-Trauma DressingNAB · Traditional Gam Industries, Inc.04/08/1993SE
K926072K-Band and K-CrepeNAB · Traditional Parema , Ltd.03/19/1993SE
K915591Sterile Gauze PadsNAB · Traditional Eagle Medical, Inc.01/27/1993SE
K924650Gauze SpongesNAB · Traditional Dav-Mar Medical Products, Inc.01/11/1993SE
K923602Absorbent Pad -- ModificationNAB · Traditional Winfield Laboratories, Inc.12/07/1992SE
K923115ClinisorbNAB · Traditional Hermitage Hospital Products, Inc.11/23/1992SE
K923378Usp Type Vii Gauze SpongesNAB · Traditional E.W.A., Ltd.10/06/1992SE

More from E.W.A., Ltd.

510(k)DeviceDecision
K926280Standard Nebulizer HeaterCAF · Traditional 03/22/1994SE
K930270Patient Preoperative Prep Tray, Single UseLRO · Traditional 02/17/1994SE
K920292Various Kits and TraysLRO · Traditional 01/26/1994SEKD
K862010Chick Surgical LightFTA · Traditional 06/09/1986SE
K860739Chick Surigical LightFSY · Traditional 03/28/1986SE
K834478Chick/Reison Patient Emerg. TrolleyKXJ · Traditional 02/21/1984SE
K830825Yield Non-Adherent DressingFRO · Traditional 05/13/1983SE
K822713Derm-A-Tec Skin Barrier Film · Traditional 12/07/1982SE

Questions and answers

When was Aegis Non-Adherent Dressing cleared by the FDA?

Aegis Non-Adherent Dressing (K820413) received a 510(k) decision of Substantially Equivalent on March 12, 1982, 28 days after the submission was received.

What is the product code of K820413?

The FDA product code is NAB – Gauze / Sponge,Nonresorbable For External Use, a Class I (low risk) device regulated under 21 CFR 878.4014.