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FDA 510(k)

SENZZZZZ AWAY

K-Number: K120176 · 2012-07-25

ApplicantCentrix, Inc.
Decision Date2012-07-25
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SENZZZZZ AWAY is the device name listed in this FDA 510(k) record. The listed applicant is Centrix, Inc.. It received FDA 510(k) clearance on 2012-07-25 under 510(k) number K120176. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENZZZZZ AWAY?

SENZZZZZ AWAY is a medical device that received FDA 510(k) clearance on 2012-07-25. The listed applicant is Centrix, Inc.. The 510(k) number is K120176.

When did SENZZZZZ AWAY receive FDA 510(k) clearance?

SENZZZZZ AWAY received FDA 510(k) clearance on 2012-07-25, under 510(k) number K120176.

Who is the listed applicant for SENZZZZZ AWAY?

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

What is the FDA product code for SENZZZZZ AWAY?

The FDA product code for SENZZZZZ AWAY is LBH.

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Other records listing Centrix, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: LBH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

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

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