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)

TIMEOSCOPE AND FLEXISCOPE

K-Number: K924095 · 1992-10-20

ApplicantStethoscopes of America, Inc.
Decision Date1992-10-20
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TIMEOSCOPE AND FLEXISCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Stethoscopes of America, Inc.. It received FDA 510(k) clearance on 1992-10-20 under 510(k) number K924095. 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 TIMEOSCOPE AND FLEXISCOPE?

TIMEOSCOPE AND FLEXISCOPE is a medical device that received FDA 510(k) clearance on 1992-10-20. The listed applicant is Stethoscopes of America, Inc.. The 510(k) number is K924095.

When did TIMEOSCOPE AND FLEXISCOPE receive FDA 510(k) clearance?

TIMEOSCOPE AND FLEXISCOPE received FDA 510(k) clearance on 1992-10-20, under 510(k) number K924095.

Who is the listed applicant for TIMEOSCOPE AND FLEXISCOPE?

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

What is the FDA product code for TIMEOSCOPE AND FLEXISCOPE?

The FDA product code for TIMEOSCOPE AND FLEXISCOPE 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

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.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.

↑