Cleared Traditional

K851734 - OMNIMED SUPERIOR TRANSDUCER PROTECTOR

K851734 is an FDA 510(k) clearance for OMNIMED SUPERIOR TRANSDUCER PROTECTOR, manufactured by Omni Intl., Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FIB cleared through the Traditional 510(k) pathway after a 28-day FDA review.

K851734 · Omni Intl., Inc. · Gastroenterology & Urology device
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May 1985
Decision
28d
Days
Class 2
Risk

K851734 is an FDA 510(k) clearance for the OMNIMED SUPERIOR TRANSDUCER PROTECTOR. Classified as Protector, Transducer, Dialysis (product code FIB), Class II - Special Controls.

Submitted by Omni Intl., Inc. (Palm Springs, US). The FDA issued a Cleared decision on May 23, 1985 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5820 - 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: 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 Omni Intl., Inc. devices

FDA 510(k) Submission Details - K851734

510(k) Number K851734 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 25, 1985
Decision Date May 23, 1985
Days to Decision 28 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
103d faster than avg
Panel avg: 131d · This submission: 28d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FIB Device Classification - Class 2, Special Controls

Product Code FIB Protector, Transducer, Dialysis
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5820
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 - FIB Protector, Transducer, Dialysis

All 17
Devices cleared under the same product code (FIB) and FDA review panel - the closest regulatory comparables to K851734.
TRANSDUCER PROTECTOR
K910821 · Gelman Sciences, Inc. · Aug 1991
MEDISYSTEMS TRANSDUCER PROTECTOR
K895856 · Medisystems Corp. · Nov 1989
DA-46 FLUID BARRIER
K891752 · Akcess Medical Products, Inc. · Apr 1989
GAMBRO PRESSURE MONITOR GUARDS
K851230 · Gambro, Inc. · Apr 1985
TRANSDUCER FILTER
K821268 · Cp Medical · Jun 1982
BACTASHIELD
K811859 · Tri-Med, Inc. · Aug 1981