Cleared Traditional

K962083 - KARL STORZ REMORGIDA FORCEPS

K962083 is an FDA 510(k) clearance for KARL STORZ REMORGIDA FORCEPS, manufactured by KARL STORZ Endoscopy-America, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code KNS cleared through the Traditional 510(k) pathway after a 156-day FDA review.

K962083 · KARL STORZ Endoscopy-America, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1996
Decision
156d
Days
Class 2
Risk

K962083 is an FDA 510(k) clearance for the KARL STORZ REMORGIDA FORCEPS. Classified as Unit, Electrosurgical, Endoscopic (with Or Without Accessories) (product code KNS), Class II - Special Controls.

Submitted by KARL STORZ Endoscopy-America, Inc. (Culver City, US). The FDA issued a Cleared decision on November 1, 1996 after a review of 156 days - an extended review cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.4300 - 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 KARL STORZ Endoscopy-America, Inc. devices

FDA 510(k) Submission Details - K962083

510(k) Number K962083 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 29, 1996
Decision Date November 01, 1996
Days to Decision 156 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
25d slower than avg
Panel avg: 131d · This submission: 156d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KNS Device Classification - Class 2, Special Controls

Product Code KNS Unit, Electrosurgical, Endoscopic (with Or Without Accessories)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.4300
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 - KNS Unit, Electrosurgical, Endoscopic (with Or Without Accessories)

All 151
Devices cleared under the same product code (KNS) and FDA review panel - the closest regulatory comparables to K962083.
MICROVASIVE GOLD PROBE
K970278 · Boston Scientific Corp · Apr 1997
ULTRATOMERX
K970053 · Boston Scientific Corp · Mar 1997
BARD HIGH FLOW PAPILLOTOME
K963484 · Bard Interventional Products Div. · Nov 1996
PAPILLOTOME
K962346 · United States Endoscopy Group, Inc. · Aug 1996
SPHINCTEROTOME
K960231 · Lighthouse Medical, Inc. · Jul 1996
REUSABLE ENDOSCOPIC ACCESSORY HANDLE
K961762 · United States Endoscopy Group, Inc. · Jul 1996