Cleared Traditional

K854911 - PERCUTANEOUS NEPHROSTOMY SETS (SCHULLER)

K854911 is an FDA 510(k) clearance for PERCUTANEOUS NEPHROSTOMY SETS (SCHULLER), manufactured by Angiomed U.S., Inc.. The device is a Class 1 General & Plastic Surgery device with product code GBO cleared through the Traditional 510(k) pathway after a 46-day FDA review.

K854911 · Angiomed U.S., Inc. · General & Plastic Surgery device
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Jan 1986
Decision
46d
Days
Class 1
Risk

K854911 is an FDA 510(k) clearance for the PERCUTANEOUS NEPHROSTOMY SETS (SCHULLER). Classified as Catheter, Nephrostomy, General & Plastic Surgery (product code GBO), Class I - General Controls.

Submitted by Angiomed U.S., Inc. (Anaheim, US). The FDA issued a Cleared decision on January 24, 1986 after a review of 46 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4200 - the FDA general and plastic surgery 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 Angiomed U.S., Inc. devices

FDA 510(k) Submission Details - K854911

510(k) Number K854911 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 09, 1985
Decision Date January 24, 1986
Days to Decision 46 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
69d faster than avg
Panel avg: 115d · This submission: 46d
Pathway characteristics
Predicate-based equivalence.

GBO Device Classification - Class 1, General Controls

Product Code GBO Catheter, Nephrostomy, General & Plastic Surgery
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4200
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.

Regulatory Peers - GBO Catheter, Nephrostomy, General & Plastic Surgery

All 9
Devices cleared under the same product code (GBO) and FDA review panel - the closest regulatory comparables to K854911.
PERCUTANEOUS NEPHROSTOMY SETS (OTTO)
K854906 · Angiomed U.S., Inc. · Jan 1986
PERCUTANEOUS NEPHROSTOMY SETS (GUNTHER)
K854907 · Angiomed U.S., Inc. · Jan 1986
PEDIATRIC PERCUTANEOUS NEPHROSTOMY SETS
K854909 · Angiomed U.S., Inc. · Jan 1986
PERCUTANEOUS NEPHROSTOMY SET
K820867 · Van-Tec, Inc. · Apr 1982
SILASTIC NEPHROSTOMY SYSTEM
K781664 · Dow Corning Corp. Healthcare Industries Materials · Jan 1979
SILASTIC U-TUBE KIT
K781526 · Dow Corning Corp. Healthcare Industries Materials · Sep 1978