Cleared Traditional

K800424 - LUNDIA PLATE DISP.

K800424 is an FDA 510(k) clearance for LUNDIA PLATE DISP., manufactured by Gambro, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FJG cleared through the Traditional 510(k) pathway after a 44-day FDA review.

K800424 · Gambro, Inc. · Gastroenterology & Urology device
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Apr 1980
Decision
44d
Days
Class 2
Risk

K800424 is an FDA 510(k) clearance for the LUNDIA PLATE DISP.. Classified as Dialyzer, Parallel Flow (product code FJG), Class II - Special Controls.

Submitted by Gambro, Inc. (Mchenry, US). The FDA issued a Cleared decision on April 10, 1980 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 Gambro, Inc. devices

FDA 510(k) Submission Details - K800424

510(k) Number K800424 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 26, 1980
Decision Date April 10, 1980
Days to Decision 44 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
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.

FJG Device Classification - Class 2, Special Controls

Product Code FJG Dialyzer, Parallel Flow
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 - FJG Dialyzer, Parallel Flow

All 23
Devices cleared under the same product code (FJG) and FDA review panel - the closest regulatory comparables to K800424.
COBE PPD .8
K810066 · Cobe Laboratories, Inc. · Jun 1981
EXTRACORPOREAL'S EXP 400 PARALLEL PLATE
K802364 · Extracorporeal Medical Specialities, Inc. · Jan 1981
GAMBRO LUNDIA PLATE DISP. DIALYZER
K802389 · Gambro, Inc. · Dec 1980
GAMBRO LUNDIA PLATE DIALYZER
K792611 · Gambro, Inc. · Feb 1980
EXTRACORPOREAL'S MODEL EX-85 DIALYZER
K791961 · Extracorporeal Medical Specialities, Inc. · Nov 1979
HEMODIALYZERS RP-510 AND RP-514
K791448 · Hospal Medical Corp. · Aug 1979