Cleared Traditional

K884920 - RECTUM-COLON MOTILITY MONITOR

K884920 is an FDA 510(k) clearance for RECTUM-COLON MOTILITY MONITOR, manufactured by Multi-Spectrum Consulting, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FAP cleared through the Traditional 510(k) pathway after a 375-day FDA review.

K884920 · Multi-Spectrum Consulting, Inc. · Gastroenterology & Urology device
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Dec 1989
Decision
375d
Days
Class 2
Risk

K884920 is an FDA 510(k) clearance for the RECTUM-COLON MOTILITY MONITOR. Classified as Cystometric Gas (carbon-dioxide) On Hydraulic Device (product code FAP), Class II - Special Controls.

Submitted by Multi-Spectrum Consulting, Inc. (Holt, US). The FDA issued a Cleared decision on December 8, 1989 after a review of 375 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1620 - the FDA gastroenterology and urology 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. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Multi-Spectrum Consulting, Inc. devices

FDA 510(k) Submission Details - K884920

510(k) Number K884920 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 28, 1988
Decision Date December 08, 1989
Days to Decision 375 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
245d slower than avg
Panel avg: 130d · This submission: 375d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FAP Device Classification - Class 2, Special Controls

Product Code FAP Cystometric Gas (carbon-dioxide) On Hydraulic Device
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1620
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - FAP Cystometric Gas (carbon-dioxide) On Hydraulic Device

All 25
Devices cleared under the same product code (FAP) and FDA review panel - the closest regulatory comparables to K884920.
URODYNAMIC RECTAL BALLOON
K912451 · Cook Urological, Inc. · Dec 1991
UROLAB JANUS
K904386 · Life-Tech Intl., Inc. · Nov 1990
BIOSEARCH ANAL BIOFEEDBACK DEVICE
K902843 · Biosearch Medical Products, Inc. · Sep 1990
SURGITEK CO2 DELIVERY SYSTEM
K881736 · Medical Engineering Corp. · Aug 1988
MODEL 4-SC FOUR WAY STOPCOCK
K863165 · Life-Tech Intl., Inc. · Oct 1986
MODEL 1350 URODYNAMIC WAVEFORM PROCESSOR
K863167 · Life-Tech Intl., Inc. · Oct 1986