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FDA 510(k)

Compound W Nitro-Freeze

K-Number: K172373 · 2017-11-02

ApplicantMedtech Products, Inc.
Decision Date2017-11-02
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Compound W Nitro-Freeze is a medical device manufactured by Medtech Products, Inc.. It received FDA 510(k) clearance on 2017-11-02 under approval number K172373. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Compound W Nitro-Freeze?

Compound W Nitro-Freeze is a medical device that received FDA 510(k) clearance on 2017-11-02. It is manufactured by Medtech Products, Inc.. The 510(k) number is K172373.

When was Compound W Nitro-Freeze approved by the FDA?

Compound W Nitro-Freeze received FDA 510(k) clearance on 2017-11-02, under approval number K172373.

What company makes Compound W Nitro-Freeze?

Compound W Nitro-Freeze is manufactured by Medtech Products, Inc..

What is the FDA product code for Compound W Nitro-Freeze?

The FDA product code for Compound W Nitro-Freeze is GEH.

Other Devices by Medtech Products, Inc.

K161294Compound W Wart Removal System Dual Power K163401Nix Ultra Lice Treatment Kit K180933DenTek Ultimate Dental Guard K202974DenTek Fresh Protect Dental Guard K242803Compound W Skin Tag Remover

Related Devices (Code: GEH)

K162695truFreeze SystemCSA Medical, Inc. K162599IcePearl 2.1 CX L, IceForce 2.1 CX LGalil Medical , Ltd. K161480R2 Dermal Cooling SystemR2 Dermatology K161294Compound W Wart Removal System Dual PowerMedtech Products, Inc. K161615AccurettH&O Equipments, Nv/Sa K161557truFreeze SystemCSA Medical, 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.

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