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FDA 510(k)

Advantage Plus Pass-Thru

K-Number: K172677 · 2017-12-19

ApplicantMedivators, Inc.
Decision Date2017-12-19
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Advantage Plus Pass-Thru is the device name listed in this FDA 510(k) record. The listed applicant is Medivators, Inc.. It received FDA 510(k) clearance on 2017-12-19 under 510(k) number K172677. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Advantage Plus Pass-Thru?

Advantage Plus Pass-Thru is a medical device that received FDA 510(k) clearance on 2017-12-19. The listed applicant is Medivators, Inc.. The 510(k) number is K172677.

When did Advantage Plus Pass-Thru receive FDA 510(k) clearance?

Advantage Plus Pass-Thru received FDA 510(k) clearance on 2017-12-19, under 510(k) number K172677.

Who is the listed applicant for Advantage Plus Pass-Thru?

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

What is the FDA product code for Advantage Plus Pass-Thru?

The FDA product code for Advantage Plus Pass-Thru is FEB.

Other records listing Medivators, Inc. as applicant

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Related Devices (Code: FEB)

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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