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FDA 510(k)

FREQUENCER, MODEL 1001

K-Number: K063645 · 2007-03-15

ApplicantDymedso, Inc.
Decision Date2007-03-15
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FREQUENCER, MODEL 1001 is the device name listed in this FDA 510(k) record. The listed applicant is Dymedso, Inc.. It received FDA 510(k) clearance on 2007-03-15 under 510(k) number K063645. 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, MODEL 1001?

FREQUENCER, MODEL 1001 is a medical device that received FDA 510(k) clearance on 2007-03-15. The listed applicant is Dymedso, Inc.. The 510(k) number is K063645.

When did FREQUENCER, MODEL 1001 receive FDA 510(k) clearance?

FREQUENCER, MODEL 1001 received FDA 510(k) clearance on 2007-03-15, under 510(k) number K063645.

Who is the listed applicant for FREQUENCER, MODEL 1001?

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, MODEL 1001?

The FDA product code for FREQUENCER, MODEL 1001 is BYI.

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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.

K103176FREQUENCERK100749FREQUENCER MODEL V2X

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.

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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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