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FDA 510(k)

PPA/BT-RB STETHOSCOPE

K-Number: K132405 · 2013-10-11

ApplicantRnk Products, Inc.
Decision Date2013-10-11
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PPA/BT-RB 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 2013-10-11 under 510(k) number K132405. 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 PPA/BT-RB STETHOSCOPE?

PPA/BT-RB STETHOSCOPE is a medical device that received FDA 510(k) clearance on 2013-10-11. The listed applicant is Rnk Products, Inc.. The 510(k) number is K132405.

When did PPA/BT-RB STETHOSCOPE receive FDA 510(k) clearance?

PPA/BT-RB STETHOSCOPE received FDA 510(k) clearance on 2013-10-11, under 510(k) number K132405.

Who is the listed applicant for PPA/BT-RB 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 PPA/BT-RB STETHOSCOPE?

The FDA product code for PPA/BT-RB 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.

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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.

K132560PCP-USB STETHOSCOPEK102893PCP/PC 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

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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