Cleared Abbreviated

K031432 - KLEIN SURGICAL INFILTRATION PUMP, MODEL KIP-II

K031432 is an FDA 510(k) clearance for KLEIN SURGICAL INFILTRATION PUMP, manufactured by Hk Surgical, Inc.. The device is a Class 2 General Hospital device with product code FRN cleared through the Abbreviated 510(k) pathway after a 93-day FDA review.

K031432 · Hk Surgical, Inc. · General Hospital
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Aug 2003
Decision
93d
Days
Class 2
Risk

K031432 is an FDA 510(k) clearance for the KLEIN SURGICAL INFILTRATION PUMP, MODEL KIP-II. Classified as Pump, Infusion (product code FRN), Class II - Special Controls.

Submitted by Hk Surgical, Inc. (Oceanside, US). The FDA issued a Cleared decision on August 7, 2003 after a review of 93 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5725 - 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 Hk Surgical, Inc. devices

FDA 510(k) Submission Details - K031432

510(k) Number K031432 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 2003
Decision Date August 07, 2003
Days to Decision 93 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
36d faster than avg
Panel avg: 129d · This submission: 93d
Pathway characteristics
Standards-based clearance path.

FRN Device Classification - Class 2, Special Controls

Product Code FRN Pump, Infusion
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5725
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 - FRN Pump, Infusion

All 500
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