Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ARGYLE ESOPHAGEAL STETHOSCOPE

K-Number: K790523 · 1979-03-27

ApplicantSherwood Medical Industries
Decision Date1979-03-27
Product CodeBZW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARGYLE ESOPHAGEAL STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1979-03-27 under 510(k) number K790523. The device is classified under product code BZW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE ESOPHAGEAL STETHOSCOPE?

ARGYLE ESOPHAGEAL STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1979-03-27. The listed applicant is Sherwood Medical Industries. The 510(k) number is K790523.

When did ARGYLE ESOPHAGEAL STETHOSCOPE receive FDA 510(k) clearance?

ARGYLE ESOPHAGEAL STETHOSCOPE received FDA 510(k) clearance on 1979-03-27, under 510(k) number K790523.

Who is the listed applicant for ARGYLE ESOPHAGEAL STETHOSCOPE?

The FDA 510(k) record lists Sherwood Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARGYLE ESOPHAGEAL STETHOSCOPE?

The FDA product code for ARGYLE ESOPHAGEAL STETHOSCOPE is BZW.

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 Sherwood Medical Industries 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.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790196MONOJECT ARTERIAL BLOOD SAMPLING DEVICE

View all 62 devices →

Related Devices (Code: BZW)

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.

K874519MODIFIED ESOPHAGEAL STETHOSCOPE/TEMPERATURE SENSORMon-A-Therm, Inc.K860558ESOPHAGEAL STETHOSCOPESharn, Inc.K844444ESOPHAGEAL STETHOSCOPEMedical Parameters, Inc.K843070ESOPHAGEAL STETHOSCOPESPrimrose Medical, Inc.K842865ESOPHAGEAL STETHOSCOPEInmed Corp.K841574QUAZAR ESOPHAGEAL STETHOSCOPEAxiom Medical, 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.

↑