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FDA 510(k)

VARIOUS STETHOSCOPES

K-Number: K944337 · 1994-11-30

ApplicantRud Riester GmbH & CO KG
Decision Date1994-11-30
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VARIOUS STETHOSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is Rud Riester GmbH & CO KG. It received FDA 510(k) clearance on 1994-11-30 under 510(k) number K944337. 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 VARIOUS STETHOSCOPES?

VARIOUS STETHOSCOPES is a medical device that received FDA 510(k) clearance on 1994-11-30. The listed applicant is Rud Riester GmbH & CO KG. The 510(k) number is K944337.

When did VARIOUS STETHOSCOPES receive FDA 510(k) clearance?

VARIOUS STETHOSCOPES received FDA 510(k) clearance on 1994-11-30, under 510(k) number K944337.

Who is the listed applicant for VARIOUS STETHOSCOPES?

The FDA 510(k) record lists Rud Riester GmbH & CO KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARIOUS STETHOSCOPES?

The FDA product code for VARIOUS STETHOSCOPES 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 Rud Riester GmbH & CO KG 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.

K942649MINIMUS I; MINIMUS III, SANAPHONK942650BIG BENK943461VARIOUS TYPES OF MERCURIALS

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.K940578MANUAL STETOSCOPEBhs Intl., Inc.K935944PROSCOPES AND ADSCOPESAmerican Diagnostic Corp.K923327STETHOSCOPE COVERAnup Chakraborty Co.K924095TIMEOSCOPE AND FLEXISCOPEStethoscopes of America, Inc.K914100STETHOSCOPEAtlas Medical Products, Inc.

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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