FDA 510(k)

VASOGRAPH, MODEL MV-2

K-Number: K822455 · 1982-09-24

Decision Date1982-09-24

Product CodeDSB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

VASOGRAPH, MODEL MV-2 is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Diagnostic Instruments. It received FDA 510(k) clearance on 1982-09-24 under 510(k) number K822455. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASOGRAPH, MODEL MV-2?

VASOGRAPH, MODEL MV-2 is a medical device that received FDA 510(k) clearance on 1982-09-24. The listed applicant is Electro-Diagnostic Instruments. The 510(k) number is K822455.

When did VASOGRAPH, MODEL MV-2 receive FDA 510(k) clearance?

VASOGRAPH, MODEL MV-2 received FDA 510(k) clearance on 1982-09-24, under 510(k) number K822455.

Who is the listed applicant for VASOGRAPH, MODEL MV-2?

The FDA 510(k) record lists Electro-Diagnostic Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASOGRAPH, MODEL MV-2?

The FDA product code for VASOGRAPH, MODEL MV-2 is DSB.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Electro-Diagnostic Instruments as applicant

K932438MODEL IPM-1 IMPEDANCE PULSE MONITOR K871912PV-LAB, MODEL PVL-1, PERIPHERAL VASCULAR SYSTEM K862714BILATERAL IMPEDANCE PLETHYSMOGRAPH, BIP(TM)

Related Devices (Code: DSB)

K260224MySOZO Software version 6.1.0.1 (SW version 6.1.0.1)ImpediMed Limited K250634BCM2-Body Composition MonitorFresenius Medical Care Renal Therapies Group, LLC K243727Re:BalansMode Sensors AS K250922Edema Guard Monitor (EGM) CardioSet-001Cardioset Medical , Ltd.K232089SOZO ProImpediMed Limited K223217Zynex Monitoring System, Model CM-1600Zynex 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.