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FDA 510(k)

PCP/PC STETHOSCOPE

K-Number: K102893 · 2011-01-20

ApplicantRnk Products, Inc.
Decision Date2011-01-20
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PCP/PC 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 2011-01-20 under 510(k) number K102893. 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 PCP/PC STETHOSCOPE?

PCP/PC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 2011-01-20. The listed applicant is Rnk Products, Inc.. The 510(k) number is K102893.

When did PCP/PC STETHOSCOPE receive FDA 510(k) clearance?

PCP/PC STETHOSCOPE received FDA 510(k) clearance on 2011-01-20, under 510(k) number K102893.

Who is the listed applicant for PCP/PC 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 PCP/PC STETHOSCOPE?

The FDA product code for PCP/PC 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 STETHOSCOPEK081032TR-USB TELEPHONIC STETHOSCOPEK072026RNK ELECTRONIC 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

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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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