Cleared Abbreviated

K060082 - TIANJIN MEDIS DISPOSABLE INFUSION SET

K060082 is an FDA 510(k) clearance for TIANJIN MEDIS DISPOSABLE INFUSION SET, manufactured by Tianjin Medis International Trade Co., Ltd.. The device is a Class 2 General Hospital device with product code FPA cleared through the Abbreviated 510(k) pathway after a 80-day FDA review.

K060082 · Tianjin Medis International Trade Co., Ltd. · General Hospital
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Mar 2006
Decision
80d
Days
Class 2
Risk

K060082 is an FDA 510(k) clearance for the TIANJIN MEDIS DISPOSABLE INFUSION SET. Classified as Set, Administration, Intravascular (product code FPA), Class II - Special Controls.

Submitted by Tianjin Medis International Trade Co., Ltd. (Hexi District, Tianjin, CN). The FDA issued a Cleared decision on March 31, 2006 after a review of 80 days - a notably fast clearance cycle.

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 Tianjin Medis International Trade Co., Ltd. devices

FDA 510(k) Submission Details - K060082

510(k) Number K060082 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 10, 2006
Decision Date March 31, 2006
Days to Decision 80 days
Submission Type Abbreviated
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
49d faster than avg
Panel avg: 129d · This submission: 80d
Pathway characteristics
Standards-based clearance path.

FPA Device Classification - Class 2, Special Controls

Product Code FPA Set, Administration, Intravascular
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 - FPA Set, Administration, Intravascular

All 708
Devices cleared under the same product code (FPA) and FDA review panel - the closest regulatory comparables to K060082.
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K053106 · Icu Medical, Inc. · Jan 2006
SURFLO WINGED INFUSION SET WITH NEEDLE PROTECTION (SURSHIELD), MODEL SV-S23BL35VS
K052887 · Terumo Europe N.V. · Dec 2005