Cleared Traditional

K093796 - ASEPT PERITONEAL DRAINAGE SYSTEM (FDA 510(k) Clearance)

Class II Gastroenterology & Urology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K093796 · Pfm Medical, Inc. · Gastroenterology & Urology device
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Feb 2010
Decision
77d
Days
Class 2
Risk

K093796 is an FDA 510(k) clearance for the ASEPT PERITONEAL DRAINAGE SYSTEM. Classified as Peritoneal, Drainage Catheter For Refractory Ascites, Long-term Indwelling (product code PNG), Class II - Special Controls.

Submitted by Pfm Medical, Inc. (Oceanside, US). The FDA issued a Cleared decision on February 26, 2010 after a review of 77 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5630 - 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 Pfm Medical, Inc. devices

Submission Details

510(k) Number K093796 FDA.gov
FDA Decision Cleared Substantially Equivalent - Special 510(k) (SESK)
Date Received December 11, 2009
Decision Date February 26, 2010
Days to Decision 77 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 130d · This submission: 77d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code PNG Peritoneal, Drainage Catheter For Refractory Ascites, Long-term Indwelling
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5630
Definition For Drainage Of Refractory Ascites With Long-term Occurrence From The Peritoneal Cavity.
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 - PNG Peritoneal, Drainage Catheter For Refractory Ascites, Long-term Indwelling

All 14
Devices cleared under the same product code (PNG) and FDA review panel - the closest regulatory comparables to K093796.
ASEPT® Glide Peritoneal Drainage System
K241278 · Pfm Medical, Inc. · Jan 2025
PeritX™ 1L Drainage Kit (90-1010)
K241946 · Bard Peripheral Vascular, Inc. · Dec 2024
ASEPT Peritoneal Drainage System
K221779 · Pfm Medical, Inc. · May 2023
Aspira Peritoneal Drainage System
K212675 · Merit Medical Systems, Inc. · Dec 2021