FDA 510(k)

Atteris No-Sting Skin Protectant

K-Number: K160684 · 2016-07-26

Decision Date2016-07-26

Product CodeKMF

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

Atteris No-Sting Skin Protectant is a medical device manufactured by Rochal Industries, LLC. It received FDA 510(k) clearance on 2016-07-26 under approval number K160684. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Atteris No-Sting Skin Protectant?

Atteris No-Sting Skin Protectant is a medical device that received FDA 510(k) clearance on 2016-07-26. It is manufactured by Rochal Industries, LLC. The 510(k) number is K160684.

When was Atteris No-Sting Skin Protectant approved by the FDA?

Atteris No-Sting Skin Protectant received FDA 510(k) clearance on 2016-07-26, under approval number K160684.

What company makes Atteris No-Sting Skin Protectant?

Atteris No-Sting Skin Protectant is manufactured by Rochal Industries, LLC.

What is the FDA product code for Atteris No-Sting Skin Protectant?

The FDA product code for Atteris No-Sting Skin Protectant is KMF.

Other Devices by Rochal Industries, LLC

K161212Atteris Antimicrobial Skin Protectant K160192Atteris Antimicrobial Skin & Wound Cleanser K182733Rochal Bioshield Silicone Film K192527Rochal Antimicrobial Wound Gel

Related Devices (Code: KMF)

K153571Cavilon Advanced High Endurance Skin Protectant3M Healthcare K171148Aleo BME Liquid BandageAleo Bme, Inc. K182733Rochal Bioshield Silicone FilmRochal Industries, LLC K241916TearRepair Liquid Skin ProtectantOptmed, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.