Cleared Traditional

K864113 - CLYDE (TM) FILTRATION SYSTEM

K864113 is an FDA 510(k) clearance for CLYDE (TM) FILTRATION SYSTEM, manufactured by Arbor Technologies, Inc.. The device is a Class 2 General Hospital device with product code FPB cleared through the Traditional 510(k) pathway after a 106-day FDA review.

K864113 · Arbor Technologies, Inc. · General Hospital
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Feb 1987
Decision
106d
Days
Class 2
Risk

K864113 is an FDA 510(k) clearance for the CLYDE (TM) FILTRATION SYSTEM. Classified as Filter, Infusion Line (product code FPB), Class II - Special Controls.

Submitted by Arbor Technologies, Inc. (Ann Arbor, US). The FDA issued a Cleared decision on February 4, 1987 after a review of 106 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5440 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Arbor Technologies, Inc. devices

FDA 510(k) Submission Details - K864113

510(k) Number K864113 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 21, 1986
Decision Date February 04, 1987
Days to Decision 106 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
23d faster than avg
Panel avg: 129d · This submission: 106d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FPB Device Classification - Class 2, Special Controls

Product Code FPB Filter, Infusion Line
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5440
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 - FPB Filter, Infusion Line

All 72
Devices cleared under the same product code (FPB) and FDA review panel - the closest regulatory comparables to K864113.
CHURCHILL 1.2 MICRON LIQUID FILTER SET
K880027 · Churchill Corp. · Apr 1988
CUTTER PUREFLO PLUS IV FILTER
K872634 · Miles Laboratories, Inc. · Aug 1987
CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER
K865029 · Travenol Laboratories, S.A. · Apr 1987
CRITIKON 48-HOUR AIR ELIMINATING FILTER
K861644 · Critikon Company, LLC · Jul 1986
IV FILTER EXTENSION SET
K860803 · Med Fusion Systems, Inc. · Apr 1986
AUTO SYRINGE MICRO VOL EXT SET W/AIR VENT FILTER
K860746 · Travenol Laboratories, S.A. · Apr 1986