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FDA 510(k)

Noxilizer Surgical Ruler

K-Number: K160501 · 2016-05-26

ApplicantNoxilizer, Inc.
Decision Date2016-05-26
Product CodeFTY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Noxilizer Surgical Ruler is the device name listed in this FDA 510(k) record. The listed applicant is Noxilizer, Inc.. It received FDA 510(k) clearance on 2016-05-26 under 510(k) number K160501. The device is classified under product code FTY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Noxilizer Surgical Ruler?

Noxilizer Surgical Ruler is a medical device that received FDA 510(k) clearance on 2016-05-26. The listed applicant is Noxilizer, Inc.. The 510(k) number is K160501.

When did Noxilizer Surgical Ruler receive FDA 510(k) clearance?

Noxilizer Surgical Ruler received FDA 510(k) clearance on 2016-05-26, under 510(k) number K160501.

Who is the listed applicant for Noxilizer Surgical Ruler?

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

What is the FDA product code for Noxilizer Surgical Ruler?

The FDA product code for Noxilizer Surgical Ruler is FTY.

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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