Cleared Traditional

K953713 - MANAN GENERAL UTILITY DRAINAGE CATHETER (FDA 510(k) Clearance)

K953713 · Manan Medical Products, Inc. · Gastroenterology & Urology device
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Mar 1996
Decision
251d
Days
-
Risk

K953713 is an FDA 510(k) clearance for the MANAN GENERAL UTILITY DRAINAGE CATHETER. Classified as Catheter, Nephrostomy (product code LJE).

Submitted by Manan Medical Products, Inc. (Northbrook, US). The FDA issued a Cleared decision on March 26, 1996 after a review of 251 days - an extended review cycle.

This device falls under the Gastroenterology & Urology FDA review panel. 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 Manan Medical Products, Inc. devices

Submission Details

510(k) Number K953713 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 19, 1995
Decision Date March 26, 1996
Days to Decision 251 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
121d slower than avg
Panel avg: 130d · This submission: 251d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code LJE Catheter, Nephrostomy
Device Class -

Regulatory Peers - LJE Catheter, Nephrostomy

All 55
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