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)

MEDVISION ENVIROMENT/MEDVISION 2.0

K-Number: K942861 · 1994-12-07

ApplicantEvergreen Technologies, Inc.
Decision Date1994-12-07
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDVISION ENVIROMENT/MEDVISION 2.0 is the device name listed in this FDA 510(k) record. The listed applicant is Evergreen Technologies, Inc.. It received FDA 510(k) clearance on 1994-12-07 under 510(k) number K942861. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDVISION ENVIROMENT/MEDVISION 2.0?

MEDVISION ENVIROMENT/MEDVISION 2.0 is a medical device that received FDA 510(k) clearance on 1994-12-07. The listed applicant is Evergreen Technologies, Inc.. The 510(k) number is K942861.

When did MEDVISION ENVIROMENT/MEDVISION 2.0 receive FDA 510(k) clearance?

MEDVISION ENVIROMENT/MEDVISION 2.0 received FDA 510(k) clearance on 1994-12-07, under 510(k) number K942861.

Who is the listed applicant for MEDVISION ENVIROMENT/MEDVISION 2.0?

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

What is the FDA product code for MEDVISION ENVIROMENT/MEDVISION 2.0?

The FDA product code for MEDVISION ENVIROMENT/MEDVISION 2.0 is LMD.

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 Evergreen 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.

K942860VISIONLINK DICOM MODULEK935103VISIONLINK ACR-NEMA CONVERSION UTILITIESK933372VISIONLINK INTERFILE CONVERSION SOFTWAREK933209VISIONTOOLK924178MEDVISION(TM) IMAGING SOFTWAREK921484MEDVISION

View all 7 devices →

Related Devices (Code: LMD)

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.

K994329IIVS INTEGRATED IMAGE VIEWING STATIONTerarecon,Inc.K992698STENTOR, PAGEVIEWStentor, Inc.K992426RAYPAX WEB CLINICAL SYSTEMSamsung Sds Co., Ltd.K992352ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.0Inteleradiology, Inc.K991537SAMSUNG RAYPAX SYSTEMSamsung Sds Co., Ltd.K984000STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEMSurgical Navigation Technologies, 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.

↑