Cleared Traditional

K861510 - MULTILUMEN VIAPIC CENTRAL LINE CATHETER

K861510 is the FDA 510(k) clearance for MULTILUMEN VIAPIC CENTRAL LINE CATHETER by Warner-Lambert Co.. It is a Class 2 General Hospital device (product code FOZ) cleared through the Traditional 510(k) pathway after a 47-day FDA review.

K861510 · Warner-Lambert Co. · General Hospital
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Jun 1986
Decision
47d
Days
Class 2
Risk

K861510 is an FDA 510(k) clearance for the MULTILUMEN VIAPIC CENTRAL LINE CATHETER. Classified as Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days (product code FOZ), Class II - Special Controls.

Submitted by Warner-Lambert Co. (Sandy, US). The FDA issued a Cleared decision on June 9, 1986 after a review of 47 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 Warner-Lambert Co. devices

Submission Details

510(k) Number K861510 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 23, 1986
Decision Date June 09, 1986
Days to Decision 47 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
82d faster than avg
Panel avg: 129d · This submission: 47d
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 240
Devices cleared under the same product code (FOZ) and FDA review panel - the closest regulatory comparables to K861510.
ARROW 18GA TWO-LUMEN INTRAVENOUS CATH/23GA NEEDLE
K862153 · Arrow Intl., Inc. · Dec 1986
INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT
K861725 · Parke-Davis Co. · Dec 1986
CAVAFIX, CENTRAL VENOUS CATHETER KIT
K861479 · Burron Medical Products, Inc. · Jul 1986
POLYCATH-H CATHETER
K854308 · Abbott Laboratories · Apr 1986
VIAPIC CENTRAL LINE CATHETER
K860290 · Parke-Davis Co. · Mar 1986
TERUMO SURFLO ETFE I.V. CATHETER
K854566 · Terumo Medical Corp. · Jan 1986