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)

EAGLE PATIENT MONITOR MODEL 3000/3100

K-Number: K961139 · 1996-08-09

ApplicantMarquette Electronics, Inc.
Decision Date1996-08-09
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EAGLE PATIENT MONITOR MODEL 3000/3100 is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Electronics, Inc.. It received FDA 510(k) clearance on 1996-08-09 under 510(k) number K961139. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAGLE PATIENT MONITOR MODEL 3000/3100?

EAGLE PATIENT MONITOR MODEL 3000/3100 is a medical device that received FDA 510(k) clearance on 1996-08-09. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K961139.

When did EAGLE PATIENT MONITOR MODEL 3000/3100 receive FDA 510(k) clearance?

EAGLE PATIENT MONITOR MODEL 3000/3100 received FDA 510(k) clearance on 1996-08-09, under 510(k) number K961139.

Who is the listed applicant for EAGLE PATIENT MONITOR MODEL 3000/3100?

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

What is the FDA product code for EAGLE PATIENT MONITOR MODEL 3000/3100?

The FDA product code for EAGLE PATIENT MONITOR MODEL 3000/3100 is DSI.

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 Marquette Electronics, 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.

K971868IMPACT (INFORMING MOBILE PERSONNEL AND CARE TRACKING) PAGER SYSTEMK971683WIRELESS LAN (LOCAL AREA NETWORK) - WIRELESS ETHERNETK972199SIGNAL-AVERAGED HIGH RESOLUTION P WAVE ANALYSISK962547CARDIOSERV PK963120RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEMK962827ALARM DISPLAY UNIT/PAGER-LAN SYSTEM (ADU)

View all 82 devices →

Related Devices (Code: DSI)

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.

K243349BodyGuardian Remote Monitoring System (BGRMS v3.0)Boston Scientific Cardiac Diagnostic Technologies, Inc.K250356MoMe ARC® Wireless Ambulatory ECG Monitoring and Detection System (32000)Infobionic, Inc.K240177Zio AT® device (A100A1001)iRhythm Technologies, Inc.K230265MoMe® ARC Wireless Ambulatory ECG Monitoring and Detection SystemInfobionic, Inc.K231276SmartCardia 7L PlatformSmartcardia SAK193104Unified Arrhythmia Diagnostic System PocketECG IVMedicalgorithmics S.A.

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.

↑