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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 the device name listed in this FDA 510(k) record. The listed applicant is Medtech Products, Inc.. It received FDA 510(k) clearance on 2017-11-02 under 510(k) 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. The listed applicant is Medtech Products, Inc.. The 510(k) number is K172373.

When did Compound W Nitro-Freeze receive FDA 510(k) clearance?

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

Who is the listed applicant for Compound W Nitro-Freeze?

The FDA 510(k) record lists Medtech Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

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Official Source

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