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)

VENTED VIAL ADAPTER TRANSFER DEVICE

K-Number: K062482 · 2006-11-03

ApplicantMedimop Medical Projects, Ltd.
Decision Date2006-11-03
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VENTED VIAL ADAPTER TRANSFER DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Medimop Medical Projects, Ltd.. It received FDA 510(k) clearance on 2006-11-03 under 510(k) number K062482. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTED VIAL ADAPTER TRANSFER DEVICE?

VENTED VIAL ADAPTER TRANSFER DEVICE is a medical device that received FDA 510(k) clearance on 2006-11-03. The listed applicant is Medimop Medical Projects, Ltd.. The 510(k) number is K062482.

When did VENTED VIAL ADAPTER TRANSFER DEVICE receive FDA 510(k) clearance?

VENTED VIAL ADAPTER TRANSFER DEVICE received FDA 510(k) clearance on 2006-11-03, under 510(k) number K062482.

Who is the listed applicant for VENTED VIAL ADAPTER TRANSFER DEVICE?

The FDA 510(k) record lists Medimop Medical Projects, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTED VIAL ADAPTER TRANSFER DEVICE?

The FDA product code for VENTED VIAL ADAPTER TRANSFER DEVICE is LHI.

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 Medimop Medical Projects, Ltd. 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.

K160503Vented Vial Adapter Transfer Device - 13mmK130179MP VIAL ADAPTER 13MMK132040VIAL CONNECTOR 13MM CLOSED COLLARK122023MIXJECT WITH SPRAY HEADK072759VIAL2BAGK072511SWABABLE VIAL ADAPTER 13MM, SWABABLE VIAL ADAPTER 20MM

View all 11 devices →

Related Devices (Code: LHI)

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.

K252987ADRx™ Admixture DeviceEpic Medical Pte. , Ltd.K260301Vial AdapterHangzhou Qiantang Longyue Biotechnology Co., Ltd.K250345Medline Bag DecanterMedline Industries, LPK251715FlowArt® Vial Access Device VentedAsset MedikalK251676Medline Microtek C-Flo Bag Decanter, Sterile (2000S); Medline Microtek Bag Decanter II, Sterile (2002S); Medline Microtek Vial Decanter, Sterile (2006S); Medline Microtek Transfer Device, Sterile (2008S)Microtek Medical, LLCK243404HyHub™ and HyHub™ Duo Vial Access DevicesTakeda Pharmaceuticals

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.

↑