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FDA 510(k)

KAMED STETHOSCOPE

K-Number: K890126 · 1989-04-21

ApplicantD.R.G.
Decision Date1989-04-21
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KAMED STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is D.R.G.. It received FDA 510(k) clearance on 1989-04-21 under 510(k) number K890126. 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 KAMED STETHOSCOPE?

KAMED STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1989-04-21. The listed applicant is D.R.G.. The 510(k) number is K890126.

When did KAMED STETHOSCOPE receive FDA 510(k) clearance?

KAMED STETHOSCOPE received FDA 510(k) clearance on 1989-04-21, under 510(k) number K890126.

Who is the listed applicant for KAMED STETHOSCOPE?

The FDA 510(k) record lists D.R.G. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KAMED STETHOSCOPE?

The FDA product code for KAMED STETHOSCOPE 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 D.R.G. 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.

K844184D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB

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 KGK940578MANUAL STETOSCOPEBhs Intl., Inc.K935944PROSCOPES AND ADSCOPESAmerican Diagnostic Corp.K923327STETHOSCOPE COVERAnup Chakraborty Co.K924095TIMEOSCOPE AND FLEXISCOPEStethoscopes of America, 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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