Cleared Traditional

K945572 - CODMAN(R) RIDIG AND STEERABLE ENDOSCOPE HOLDER, MODEL 83-1352

K945572 is an FDA 510(k) clearance for CODMAN RIDIG AND STEERABLE ENDOSCOPE HOLDER, manufactured by Johnson & Johnson Professionals, Inc.. The device is a Class 2 Neurology device with product code GWG cleared through the Traditional 510(k) pathway after a 81-day FDA review.

K945572 · Johnson & Johnson Professionals, Inc. · Neurology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1995
Decision
81d
Days
Class 2
Risk

K945572 is an FDA 510(k) clearance for the CODMAN(R) RIDIG AND STEERABLE ENDOSCOPE HOLDER, MODEL 83-1352. Classified as Endoscope, Neurological (product code GWG), Class II - Special Controls.

Submitted by Johnson & Johnson Professionals, Inc. (Raritan, US). The FDA issued a Cleared decision on February 3, 1995 after a review of 81 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1480 - the FDA neurology 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 Johnson & Johnson Professionals, Inc. devices

FDA 510(k) Submission Details - K945572

510(k) Number K945572 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 14, 1994
Decision Date February 03, 1995
Days to Decision 81 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
67d faster than avg
Panel avg: 148d · This submission: 81d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GWG Device Classification - Class 2, Special Controls

Product Code GWG Endoscope, Neurological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1480
Definition If The Device Is Reusable, Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission (82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
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 Neurology devices follow this clearance model.

Regulatory Peers - GWG Endoscope, Neurological

All 87
Devices cleared under the same product code (GWG) and FDA review panel - the closest regulatory comparables to K945572.
CLARUS PHOENIX NEURO ENDOSCOPE MODEL 2160
K945296 · Clarus Medical Systems, Inc. · Jul 1995
1.2MM DISPOSABLE NEUROVIEW(TM) PERFORMED ENDOSCOPE AND ACCESSORIES
K950154 · Neuro Navigational Corp. · Jul 1995
DISPOSABLE ASPIRATION/IRRIGATION CATHETER
K934154 · Neuro Navigational Corp. · Feb 1995
CLARUS ENDOSCOPIC NEUROLOGICAL TISSUE ELEVATOR
K942413 · Clarus Medical Systems, Inc. · Nov 1994
CLARUS NEUROPEN MODEL 2120
K942249 · Clarus Medical Systems, Inc. · Nov 1994
DISPOSABLE BIPOLAR ELECTRODE
K942955 · Neuro Navigational Corp. · Aug 1994