Cleared Traditional

K850369 - QUINTON WHITE SEALING CAP

K850369 is the FDA 510(k) clearance for QUINTON WHITE SEALING CAP by Quinton, Inc.. It is a Class 2 General Hospital device (product code FOZ) cleared through the Traditional 510(k) pathway after a 15-day FDA review.

K850369 · Quinton, Inc. · General Hospital
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Feb 1985
Decision
15d
Days
Class 2
Risk

K850369 is an FDA 510(k) clearance for the QUINTON WHITE SEALING CAP. Classified as Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days (product code FOZ), Class II - Special Controls.

Submitted by Quinton, Inc. (Seattle, US). The FDA issued a Cleared decision on February 15, 1985 after a review of 15 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 Quinton, Inc. devices

Submission Details

510(k) Number K850369 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 31, 1985
Decision Date February 15, 1985
Days to Decision 15 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
114d faster than avg
Panel avg: 129d · This submission: 15d
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 271
Devices cleared under the same product code (FOZ) and FDA review panel - the closest regulatory comparables to K850369.
DESERET ARTERIAL CATHETER
K851327 · Parke-Davis Co. · Jun 1985
SPECTRUM(TENTATIVE)
K852078 · Parke-Davis Co. · Jun 1985
QUINTON INJECTION SEALING CAP
K844193 · Quinton, Inc. · May 1985
DESERET INTRAVASCULAR CATHETER
K843033 · Parke-Davis Co. · Dec 1984
DESERET SUBCLAVIAN JUGULAR CATHETER SET
K844113 · Parke-Davis Co. · Nov 1984
DESERET DENTRAL LINE CATHETER
K844219 · Parke-Davis Co. · Nov 1984