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FDA 510(k)

RNK TELEPHONIC STETHOSCOPE, MODEL TR-1

K-Number: K034046 · 2004-03-10

ApplicantRnk Products
Decision Date2004-03-10
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RNK TELEPHONIC STETHOSCOPE, MODEL TR-1 is the device name listed in this FDA 510(k) record. The listed applicant is Rnk Products. It received FDA 510(k) clearance on 2004-03-10 under 510(k) number K034046. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RNK TELEPHONIC STETHOSCOPE, MODEL TR-1?

RNK TELEPHONIC STETHOSCOPE, MODEL TR-1 is a medical device that received FDA 510(k) clearance on 2004-03-10. The listed applicant is Rnk Products. The 510(k) number is K034046.

When did RNK TELEPHONIC STETHOSCOPE, MODEL TR-1 receive FDA 510(k) clearance?

RNK TELEPHONIC STETHOSCOPE, MODEL TR-1 received FDA 510(k) clearance on 2004-03-10, under 510(k) number K034046.

Who is the listed applicant for RNK TELEPHONIC STETHOSCOPE, MODEL TR-1?

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

What is the FDA product code for RNK TELEPHONIC STETHOSCOPE, MODEL TR-1?

The FDA product code for RNK TELEPHONIC STETHOSCOPE, MODEL TR-1 is DQD.

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Related Devices (Code: DQD)

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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