Decitel Ausculscope

FDA 510(k) K860994 · Bloomfield Research and Development, Inc.

Substantially Equivalent

510(k) numberK860994

Submission

Device name
Decitel Ausculscope
Applicant
Bloomfield Research and Development, Inc.
Hilton Head, SC, US
Received
March 17, 1986
Decision date
November 7, 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

510(k)DeviceApplicantDecision
K261494Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart…DQD · Traditional Shanghai Hulu Devices Co., Ltd.07/31/2026SE
K261694CORE 300 Digital StethoscopeDQD · Traditional Eko Health, Inc.07/23/2026SE
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
K860992Vox CompanionESE · Traditional 05/02/1986SE
K860993P.O. VoxESE · Traditional 04/25/1986SE

Questions and answers

When was Decitel Ausculscope cleared by the FDA?

Decitel Ausculscope (K860994) received a 510(k) decision of Substantially Equivalent on November 7, 1986, 235 days after the submission was received.

What is the product code of K860994?

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