Transcor (TM) Radio-Stethoscope

FDA 510(k) K854772 · K & S Medicorp

Substantially Equivalent

510(k) numberK854772

Submission

Device name
Transcor (TM) Radio-Stethoscope
Applicant
K & S Medicorp
Miami, FL, US
Received
November 29, 1985
Decision date
May 13, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DQD – Stethoscope, Electronic
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1875
Specialty
Cardiovascular

Other 510(k)s with product code DQD

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K252915AiSteth®DQD · Traditional Ai Health Highway India Pvt., Ltd.05/22/2026SE
K252089Tyto Stethoscope (G3)DQD · Traditional Tyto Care , Ltd.03/12/2026SE
K252076Kneevoice Cartilage Evaluation System (750-3600-001)DQD · Traditional Kneevoice, Inc.02/06/2026SE
K252284eMurmur Heart AIDQD · Traditional Csd Labs12/19/2025SE
K252595Stethophone ProDQD · Special Sparrow Acoustics, Inc.09/12/2025SE
K251494Eko Foundation Analysis Software with Transformers (EFAST)DQD · Traditional Eko Health, Inc.08/12/2025SE
K242971AccurSound Electronic Stethoscope (AS101)DQD · Traditional Heroic Faith International , Ltd.11/25/2024SE
K240901StethophoneDQD · Traditional Sparrow Acoustics, Inc.09/19/2024SE

More from Sparrow Acoustics, Inc.

510(k)DeviceDecision
K862131Saltzman Ear(Tm) Endotracheal Ascultation ReceptorBZT · Traditional 07/14/1986SE
K854771Saltzman Stethoscope HeadLDE · Traditional 05/09/1986SE

Questions and answers

When was Transcor (TM) Radio-Stethoscope cleared by the FDA?

Transcor (TM) Radio-Stethoscope (K854772) received a 510(k) decision of Substantially Equivalent on May 13, 1986, 165 days after the submission was received.

What is the product code of K854772?

The FDA product code is DQD – Stethoscope, Electronic, a Class II (moderate risk) device regulated under 21 CFR 870.1875.