Cleared Traditional

K914475 - IV START KIT

K914475 is an FDA 510(k) clearance for IV START KIT, manufactured by Cypress Medical Products, Ltd.. The device is a Class 2 General & Plastic Surgery device with product code LRS cleared through the Traditional 510(k) pathway after a 162-day FDA review.

K914475 · Cypress Medical Products, Ltd. · General & Plastic Surgery device
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Mar 1992
Decision
162d
Days
Class 2
Risk

K914475 is an FDA 510(k) clearance for the IV START KIT. Classified as I.v. Start Kit (product code LRS), Class II - Special Controls.

Submitted by Cypress Medical Products, Ltd. (Mc Henry, US). The FDA issued a Cleared decision on March 18, 1992 after a review of 162 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 880.5200 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Cypress Medical Products, Ltd. devices

FDA 510(k) Submission Details - K914475

510(k) Number K914475 FDA.gov
FDA Decision Cleared Substantially Equivalent - De Novo Granted (SEKD)
Date Received October 08, 1991
Decision Date March 18, 1992
Days to Decision 162 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
47d slower than avg
Panel avg: 115d · This submission: 162d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LRS Device Classification - Class 2, Special Controls

Product Code LRS I.v. Start Kit
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5200
Definition This Product Code Has Been Established In Accordance With The May 20, 1997, Guidance Entitled, Convenience Kits Interim Regulatory Guidance, Found At Http://www.fda.gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm080217.pdf. This Type Of Convenience Kit, As Listed In The Guidance Above, Is Under Enforcement Discretion, And Does Not Require A Premarket Notification (510(k)) To Market If It Meets All Criteria In The Guidance.
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 & Plastic Surgery devices follow this clearance model.

Regulatory Peers - LRS I.v. Start Kit

All 10
Devices cleared under the same product code (LRS) and FDA review panel - the closest regulatory comparables to K914475.
IV PREP KIT W/O DRESSING (NON-STERILE)
K925018 · Customed, Inc. · Aug 1993
COLD CD ASP MODULE, ITE
K933041 · Electone, Inc. · Aug 1993
I.V. START KIT, STERILE, DISPOSABLE
K923361 · Trinity Laboratories, Inc. · Jun 1993
I.V. START KIT, STERILE, DISPOSABLES
K863712 · Busse Hospital Disposables, Inc. · Oct 1986
CURITY I.V. START KIT
K842898 · The Kendal Co. · Aug 1984
ARGYLE IV STARTER KIT (W/O DRUG)
K760876 · Sherwood Medical Industries · Dec 1976