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FDA 510(k)

MANUAL STETOSCOPE

K-Number: K940578 · 1994-04-26

ApplicantBhs Intl., Inc.
Decision Date1994-04-26
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MANUAL STETOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Bhs Intl., Inc.. It received FDA 510(k) clearance on 1994-04-26 under 510(k) number K940578. The device is classified under product code LDE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANUAL STETOSCOPE?

MANUAL STETOSCOPE is a medical device that received FDA 510(k) clearance on 1994-04-26. The listed applicant is Bhs Intl., Inc.. The 510(k) number is K940578.

When did MANUAL STETOSCOPE receive FDA 510(k) clearance?

MANUAL STETOSCOPE received FDA 510(k) clearance on 1994-04-26, under 510(k) number K940578.

Who is the listed applicant for MANUAL STETOSCOPE?

The FDA 510(k) record lists Bhs Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MANUAL STETOSCOPE?

The FDA product code for MANUAL STETOSCOPE is LDE.

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 Bhs Intl., 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.

K000814FINGER PULSE METER

Related Devices (Code: LDE)

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.

K945082CYPRESS MEDICAL PRODUCTS STETHOSCOPECypress Medical Products, Ltd.K944337VARIOUS STETHOSCOPESRud Riester GmbH & CO KGK935944PROSCOPES AND ADSCOPESAmerican Diagnostic Corp.K923327STETHOSCOPE COVERAnup Chakraborty Co.K924095TIMEOSCOPE AND FLEXISCOPEStethoscopes of America, Inc.K914100STETHOSCOPEAtlas Medical Products, Inc.

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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