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FDA 510(k)

FREQUENCER

K-Number: K103176 · 2011-01-26

ApplicantDymedso, Inc.
Decision Date2011-01-26
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FREQUENCER is the device name listed in this FDA 510(k) record. The listed applicant is Dymedso, Inc.. It received FDA 510(k) clearance on 2011-01-26 under 510(k) number K103176. The device is classified under product code BYI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREQUENCER?

FREQUENCER is a medical device that received FDA 510(k) clearance on 2011-01-26. The listed applicant is Dymedso, Inc.. The 510(k) number is K103176.

When did FREQUENCER receive FDA 510(k) clearance?

FREQUENCER received FDA 510(k) clearance on 2011-01-26, under 510(k) number K103176.

Who is the listed applicant for FREQUENCER?

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

What is the FDA product code for FREQUENCER?

The FDA product code for FREQUENCER is BYI.

Related Clinical Trials

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.

Other records listing Dymedso, 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.

Related Devices (Code: BYI)

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.

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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