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)

M2376A DEVICELINK SYSTEM, MODEL M2376A

K-Number: K002967 · 2000-10-18

ApplicantAgilent Technologies, Inc.
Decision Date2000-10-18
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

M2376A DEVICELINK SYSTEM, MODEL M2376A is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies, Inc.. It received FDA 510(k) clearance on 2000-10-18 under 510(k) number K002967. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M2376A DEVICELINK SYSTEM, MODEL M2376A?

M2376A DEVICELINK SYSTEM, MODEL M2376A is a medical device that received FDA 510(k) clearance on 2000-10-18. The listed applicant is Agilent Technologies, Inc.. The 510(k) number is K002967.

When did M2376A DEVICELINK SYSTEM, MODEL M2376A receive FDA 510(k) clearance?

M2376A DEVICELINK SYSTEM, MODEL M2376A received FDA 510(k) clearance on 2000-10-18, under 510(k) number K002967.

Who is the listed applicant for M2376A DEVICELINK SYSTEM, MODEL M2376A?

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

What is the FDA product code for M2376A DEVICELINK SYSTEM, MODEL M2376A?

The FDA product code for M2376A DEVICELINK SYSTEM, MODEL M2376A is MWI.

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 Agilent Technologies, 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.

K163367GenetiSure Dx Postnatal AssayK012094MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376AK011824AGILENT M2636B TELEMON B MONITOR (TELEMON B)K010634HEARTSTREAM XL DEFIBIBRILLATOR/MONITOR, MODEL M4735A, HEARTSTREAM XLT DEFIBRILLATOR/MONITOR.MODEL M2500BK011578M2376A DEVICELINK SYSTEM, MODEL M2376AK003819HEARTSTREAM ATTENUATED DEFIBRILLATION PADS, MODEL M3870A

View all 30 devices →

Related Devices (Code: MWI)

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.

K260438Vital Signs Monitor (CLEO2)Infinium Medical, Inc.K253417Masimo Root Monitoring SystemMasimo CorporationK253196Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)Midmark CorporationK253436c-med0 alphaCosinuss GmbHK250135WAVE Clinical Platform (2.0.000)Baxter Healthcare Corp/ Excel MedicalK241766QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid)Fysicon BV

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.

↑