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FDA 510(k)

TRANSCOR (TM) RADIO-STETHOSCOPE

K-Number: K854772 · 1986-05-13

ApplicantK & S Medicorp
Decision Date1986-05-13
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRANSCOR (TM) RADIO-STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is K & S Medicorp. It received FDA 510(k) clearance on 1986-05-13 under 510(k) number K854772. 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 TRANSCOR (TM) RADIO-STETHOSCOPE?

TRANSCOR (TM) RADIO-STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1986-05-13. The listed applicant is K & S Medicorp. The 510(k) number is K854772.

When did TRANSCOR (TM) RADIO-STETHOSCOPE receive FDA 510(k) clearance?

TRANSCOR (TM) RADIO-STETHOSCOPE received FDA 510(k) clearance on 1986-05-13, under 510(k) number K854772.

Who is the listed applicant for TRANSCOR (TM) RADIO-STETHOSCOPE?

The FDA 510(k) record lists K & S Medicorp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSCOR (TM) RADIO-STETHOSCOPE?

The FDA product code for TRANSCOR (TM) RADIO-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 K & S Medicorp 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.

K862131SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTORK854771SALTZMAN STETHOSCOPE HEAD

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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