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FDA 510(k)

Beactive Brace

K-Number: K151476 · 2016-02-26

ApplicantNatures Pillows, Inc.
Decision Date2016-02-26
Product CodePMV
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Beactive Brace is the device name listed in this FDA 510(k) record. The listed applicant is Natures Pillows, Inc.. It received FDA 510(k) clearance on 2016-02-26 under 510(k) number K151476. The device is classified under product code PMV. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Beactive Brace?

Beactive Brace is a medical device that received FDA 510(k) clearance on 2016-02-26. The listed applicant is Natures Pillows, Inc.. The 510(k) number is K151476.

When did Beactive Brace receive FDA 510(k) clearance?

Beactive Brace received FDA 510(k) clearance on 2016-02-26, under 510(k) number K151476.

Who is the listed applicant for Beactive Brace?

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

What is the FDA product code for Beactive Brace?

The FDA product code for Beactive Brace is PMV.

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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