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FDA 510(k)

RNK ELECTRONIC STETHOSCOPE

K-Number: K072026 · 2007-10-26

ApplicantRnk Products, Inc.
Decision Date2007-10-26
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RNK ELECTRONIC STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Rnk Products, Inc.. It received FDA 510(k) clearance on 2007-10-26 under 510(k) number K072026. 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 ELECTRONIC STETHOSCOPE?

RNK ELECTRONIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 2007-10-26. The listed applicant is Rnk Products, Inc.. The 510(k) number is K072026.

When did RNK ELECTRONIC STETHOSCOPE receive FDA 510(k) clearance?

RNK ELECTRONIC STETHOSCOPE received FDA 510(k) clearance on 2007-10-26, under 510(k) number K072026.

Who is the listed applicant for RNK ELECTRONIC STETHOSCOPE?

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

What is the FDA product code for RNK ELECTRONIC STETHOSCOPE?

The FDA product code for RNK ELECTRONIC STETHOSCOPE is DQD.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Rnk Products, 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.

K132405PPA/BT-RB STETHOSCOPEK132560PCP-USB STETHOSCOPEK102893PCP/PC STETHOSCOPEK081032TR-USB TELEPHONIC STETHOSCOPE

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.

K261494Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart Wireless Stethoscope (STEMO720);Smart Wireless Stethoscope (STEMO730)Shanghai Hulu Devices Co., Ltd.K261694CORE 300 Digital StethoscopeEko Health, Inc.K252915AiSteth®Ai Health Highway India Pvt., Ltd.K252089Tyto Stethoscope (G3)Tyto Care , Ltd.K252076Kneevoice Cartilage Evaluation System (750-3600-001)Kneevoice, Inc.K252284eMurmur Heart AICsd Labs

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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