VENTED VIAL ADAPTER TRANSFER DEVICE— 510(k) K062482

Name: FDA 510(k) clearance K062482
Creator: U.S. Food and Drug Administration
Published: 2006-11-03

Substantially Equivalent

Medimop Medical Projects, Ltd.

FDA 510(k) clearance K062482 for VENTED VIAL ADAPTER TRANSFER DEVICE, Substantially Equivalent on 2006-11-03. Applicant: Medimop Medical Projects, Ltd.. Device class: 2.

Clearance details

Applicant: Medimop Medical Projects, Ltd.
Product code: Code LHI
Device class: Class 2
Regulation: 21 CFR 880.5440
Advisory panel: General Hospital
Date received: 2006-08-24
Decision date: 2006-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raanana, IL

Download summary PDF View on FDA.gov ↗

Recent devices under product code LHI

view all

K252987 — ADRx Admixture Device2026-06-12
K260301 — Vial Adapter2026-06-05
K250345 — Medline Bag Decanter2025-10-24
K251715 — FlowArt® Vial Access Device Vented2025-10-14
K251676 — Medline Microtek C-Flo Bag Decanter, Sterile (2000S) +3 more2025-09-16

More clearances from Medimop Medical Projects, Ltd.

view all

K160503 — Vented Vial Adapter Transfer Device - 13mm2016-05-04
K140730 — VIAL2BAG DIRECT CONNECT2014-06-12
K130179 — MP VIAL ADAPTER 13MM2013-08-08
K132040 — VIAL CONNECTOR 13MM CLOSED COLLAR2013-07-31
K122023 — MIXJECT WITH SPRAY HEAD2012-10-04

Adverse events under product code LHI

product code LHI

Injury: 207
Malfunction: 7,820
Other: 3
Total: 8,030

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.