Cleared Abbreviated

K072511 - SWABABLE VIAL ADAPTER 13MM, SWABABLE VIAL ADAPTER 20MM

K072511 is an FDA 510(k) clearance for SWABABLE VIAL ADAPTER 13MM, manufactured by Medimop Medical Projects, Ltd.. The device is a Class 2 General Hospital device with product code LHI cleared through the Abbreviated 510(k) pathway after a 98-day FDA review.

K072511 · Medimop Medical Projects, Ltd. · General Hospital
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Dec 2007
Decision
98d
Days
Class 2
Risk

K072511 is an FDA 510(k) clearance for the SWABABLE VIAL ADAPTER 13MM, SWABABLE VIAL ADAPTER 20MM. Classified as Set, I.v. Fluid Transfer (product code LHI), Class II - Special Controls.

Submitted by Medimop Medical Projects, Ltd. (Lionville, US). The FDA issued a Cleared decision on December 13, 2007 after a review of 98 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5440 - the FDA general hospital device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Medimop Medical Projects, Ltd. devices

FDA 510(k) Submission Details - K072511

510(k) Number K072511 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 06, 2007
Decision Date December 13, 2007
Days to Decision 98 days
Submission Type Abbreviated
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
31d faster than avg
Panel avg: 129d · This submission: 98d
Pathway characteristics
Standards-based clearance path.

LHI Device Classification - Class 2, Special Controls

Product Code LHI Set, I.v. Fluid Transfer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5440
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - LHI Set, I.v. Fluid Transfer

All 95
Devices cleared under the same product code (LHI) and FDA review panel - the closest regulatory comparables to K072511.
BAXJECT II HI-FLOW NEEDLELESS TRANSFER DEVICE
K092318 · Baxter Healthcare Corporation · Oct 2009
ADDEASE 20MM BINARY CONNECTOR WITH 17 GA. NEEDLE
K090905 · B.Braun Medical, Inc. · Apr 2009
NEXUS I.V. FLUID TRANSFER DEVICE
K080976 · Nexus Medical, LLC · Nov 2008
PINNACLE TPN MANAGEMENT SYSTEM TRANSFER SET
K041222 · B.Braun Medical, Inc. · Oct 2004
BAXJECT II
K042410 · Baxter Healthcare Corp · Oct 2004
CHEMO DISPENSING PIN, MODEL 12495
K024239 · Abbott Laboratories · Jan 2003