Cleared Traditional

K821383 - ECHO

K821383 is the FDA 510(k) clearance for ECHO by Mesa Medical, Inc.. It is a Class 2 Gastroenterology & Urology device (product code LIF) cleared through the Traditional 510(k) pathway after a 44-day FDA review.

K821383 · Mesa Medical, Inc. · Gastroenterology & Urology device
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Jun 1982
Decision
44d
Days
Class 2
Risk

K821383 is an FDA 510(k) clearance for the ECHO, MODEL MM-1000. Classified as Dialyzer Reprocessing System (product code LIF), Class II - Special Controls.

Submitted by Mesa Medical, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 23, 1982 after a review of 44 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 Mesa Medical, Inc. devices

Submission Details

510(k) Number K821383 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 10, 1982
Decision Date June 23, 1982
Days to Decision 44 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
86d faster than avg
Panel avg: 130d · This submission: 44d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code LIF Dialyzer Reprocessing System
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 - LIF Dialyzer Reprocessing System

All 12
Devices cleared under the same product code (LIF) and FDA review panel - the closest regulatory comparables to K821383.
HPR HOME PATIENT RENATRON
K833181 · Renal Systems, Inc. · Oct 1983
RENALIN (TENTATIVE
K830575 · Renal Systems, Inc. · Mar 1983
RENATRON DIALYZER REPROCESSING SYS
K830574 · Renal Systems, Inc. · Mar 1983
HYDROGEN PEROXIDE TOPICAL
K820221 · Renal Systems, Inc. · Mar 1982
MODEL RS 8300
K812230 · Renal Systems, Inc. · Nov 1981