Cleared Traditional

K870403 - CAVAFIX CENTRAL VENOUS CATHETER KIT W/S...

K870403 is the FDA 510(k) clearance for CAVAFIX CENTRAL VENOUS CATHETER KIT W/S... by Burron Medical Products, Inc.. It is a Class 2 General Hospital device (product code FOZ) cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K870403 · Burron Medical Products, Inc. · General Hospital
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May 1987
Decision
88d
Days
Class 2
Risk

K870403 is an FDA 510(k) clearance for the CAVAFIX(R) CENTRAL VENOUS CATHETER KIT W/SUTURE. Classified as Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days (product code FOZ), Class II - Special Controls.

Submitted by Burron Medical Products, Inc. (Bethlehem, US). The FDA issued a Cleared decision on May 1, 1987 after a review of 88 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5200 - the FDA general hospital 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Burron Medical Products, Inc. devices

Submission Details

510(k) Number K870403 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 02, 1987
Decision Date May 01, 1987
Days to Decision 88 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 129d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FOZ Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5200
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 - FOZ Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days

All 144
Devices cleared under the same product code (FOZ) and FDA review panel - the closest regulatory comparables to K870403.
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K881666 · Icu Medical, Inc. · May 1988
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K873050 · C.R. Bard, Inc. · Oct 1987
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K864949 · Quinton, Inc. · Feb 1987
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K862153 · Arrow Intl., Inc. · Dec 1986
POLYCATH-H CATHETER
K854308 · Abbott Laboratories · Apr 1986