FDA 510(k)

EASYDEX

K-Number: K120247 · 2012-06-21

Decision Date2012-06-21

Product CodeMRV

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

EASYDEX is the device name listed in this FDA 510(k) record. The listed applicant is Vineland Syrup, Inc.. It received FDA 510(k) clearance on 2012-06-21 under 510(k) number K120247. The device is classified under product code MRV. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYDEX?

EASYDEX is a medical device that received FDA 510(k) clearance on 2012-06-21. The listed applicant is Vineland Syrup, Inc.. The 510(k) number is K120247.

When did EASYDEX receive FDA 510(k) clearance?

EASYDEX received FDA 510(k) clearance on 2012-06-21, under 510(k) number K120247.

Who is the listed applicant for EASYDEX?

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

What is the FDA product code for EASYDEX?

The FDA product code for EASYDEX is MRV.

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

Related Devices (Code: MRV)

K042183GLUCOSE TOLERANCE BEVERAGEEver Scientific K032753GLUCOSE TOLERANCE BEVERAGEPerk Scientific, 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.