Cleared Traditional

K934585 - PRO-FLO SYSTEM WITH INFRA-RED REMOTE CONTROL (FDA 510(k) Clearance)

Class I Radiology device.

K934585 · Lafayette Pharmaceuticals, Inc. · Radiology device
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Nov 1993
Decision
41d
Days
Class 1
Risk

K934585 is an FDA 510(k) clearance for the PRO-FLO SYSTEM WITH INFRA-RED REMOTE CONTROL. Classified as Barium Enema Kit (product code FCD), Class I - General Controls.

Submitted by Lafayette Pharmaceuticals, Inc. (Lafayette, US). The FDA issued a Cleared decision on November 3, 1993 after a review of 41 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 876.5210 - the FDA radiology and imaging software oversight 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 Lafayette Pharmaceuticals, Inc. devices

Submission Details

510(k) Number K934585 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 23, 1993
Decision Date November 03, 1993
Days to Decision 41 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
66d faster than avg
Panel avg: 107d · This submission: 41d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FCD Barium Enema Kit
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 876.5210
Definition This Product Code Has Been Established In Accordance With The May 20, 1997, Guidance Entitled, Convenience Kits Interim Regulatory Guidance, Found At Www.fda.gov/cdrh/ode/convkit.html. This Type Of Convenience Kit, As Listed In The Guidance Above, Is Under Enforcement Discretion, And Does Not Require A Premarket Notification (510(k)) To Market If It Meets All Criteria In The Guidance.
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.