Cleared Traditional

K905779 - ALDETECT

K905779 is an FDA 510(k) clearance for ALDETECT, manufactured by Pochemco, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FJI cleared through the Traditional 510(k) pathway after a 147-day FDA review.

K905779 · Pochemco, Inc. · Gastroenterology & Urology device
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May 1991
Decision
147d
Days
Class 2
Risk

K905779 is an FDA 510(k) clearance for the ALDETECT. Classified as Dialyzer, Capillary, Hollow Fiber (product code FJI), Class II - Special Controls.

Submitted by Pochemco, Inc. (Chicopee, US). The FDA issued a Cleared decision on May 23, 1991 after a review of 147 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. 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 Pochemco, Inc. devices

FDA 510(k) Submission Details - K905779

510(k) Number K905779 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 27, 1990
Decision Date May 23, 1991
Days to Decision 147 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
17d slower than avg
Panel avg: 130d · This submission: 147d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FJI Device Classification - Class 2, Special Controls

Product Code FJI Dialyzer, Capillary, Hollow Fiber
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 - FJI Dialyzer, Capillary, Hollow Fiber

All 96
Devices cleared under the same product code (FJI) and FDA review panel - the closest regulatory comparables to K905779.
BAXTER CA DIALYZER
K926567 · Baxter Healthcare Corp · Jan 1995
FRESENIUS HEMOFLOW, VARIOUS MODELS
K926005 · Fresenius USA, Inc. · Aug 1994
HOLLOW FIBER DIALYZER FOCUS 9OR/90H-R/120R/120H-R
K914790 · National Medical Care, Medical Products Div., Inc. · Mar 1993
NEW COBE CENTRYSYSTEM(TM) 100 HG DIALYZER
K904566 · Cobe Laboratories, Inc. · Dec 1990
MODEL CA.150 CELLULOSE ACETATE HOLLOW FIBER DIALYZ
K905228 · Baxter Healthcare Corp · Dec 1990
BIO* NEPHROSS ANDANTE, MODERATO, ALLEGIO H.F.
K903567 · Organon Teknika Corp. · Sep 1990