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FDA 510(k)

RHYTHMLINK INTERNATIONAL MONOPOLAR STIMULATING INSTRUMENT

K-Number: K072736 · 2008-01-22

ApplicantRhythmlink International, LLC
Decision Date2008-01-22
Product CodeETN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RHYTHMLINK INTERNATIONAL MONOPOLAR STIMULATING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Rhythmlink International, LLC. It received FDA 510(k) clearance on 2008-01-22 under 510(k) number K072736. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RHYTHMLINK INTERNATIONAL MONOPOLAR STIMULATING INSTRUMENT?

RHYTHMLINK INTERNATIONAL MONOPOLAR STIMULATING INSTRUMENT is a medical device that received FDA 510(k) clearance on 2008-01-22. The listed applicant is Rhythmlink International, LLC. The 510(k) number is K072736.

When did RHYTHMLINK INTERNATIONAL MONOPOLAR STIMULATING INSTRUMENT receive FDA 510(k) clearance?

RHYTHMLINK INTERNATIONAL MONOPOLAR STIMULATING INSTRUMENT received FDA 510(k) clearance on 2008-01-22, under 510(k) number K072736.

Who is the listed applicant for RHYTHMLINK INTERNATIONAL MONOPOLAR STIMULATING INSTRUMENT?

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

What is the FDA product code for RHYTHMLINK INTERNATIONAL MONOPOLAR STIMULATING INSTRUMENT?

The FDA product code for RHYTHMLINK INTERNATIONAL MONOPOLAR STIMULATING INSTRUMENT is ETN.

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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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