Cleared Traditional

K973252 - KARL STORZ DIRECT COUPLED CAMERA HEAD

K973252 is an FDA 510(k) clearance for KARL STORZ DIRECT COUPLED CAMERA HEAD, manufactured by Karl Storz Imaging, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FET cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K973252 · Karl Storz Imaging, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1997
Decision
87d
Days
Class 2
Risk

K973252 is an FDA 510(k) clearance for the KARL STORZ DIRECT COUPLED CAMERA HEAD. Classified as Endoscopic Video Imaging System/component, Gastroenterology-urology (product code FET), Class II - Special Controls.

Submitted by Karl Storz Imaging, Inc. (Goleta, US). The FDA issued a Cleared decision on November 24, 1997 after a review of 87 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1500 - 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 Karl Storz Imaging, Inc. devices

FDA 510(k) Submission Details - K973252

510(k) Number K973252 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 29, 1997
Decision Date November 24, 1997
Days to Decision 87 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
44d faster than avg
Panel avg: 131d · This submission: 87d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FET Device Classification - Class 2, Special Controls

Product Code FET Endoscopic Video Imaging System/component, Gastroenterology-urology
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Allow For Visualization Of Body Cavities Through An Endoscope By Projecting Images To A Monitor.
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 - FET Endoscopic Video Imaging System/component, Gastroenterology-urology

All 73
Devices cleared under the same product code (FET) and FDA review panel - the closest regulatory comparables to K973252.
MAGNA-CAM (MR ENDOSCOPIC CAMERA) AND MAGNA-PIX ( MR COLOR VIDEO MONITOR)
K981856 · Greatbatch Scientific · Jul 1998
VES 0281-M COMPLETE VIDEO ENDOSCOPIC VIDEO SYSTEM
K981827 · Angiolaz, Inc. · Jul 1998
S-357 VIDEO IMAGING SYSTEM
K973798 · Sopro · Dec 1997
S-357 VIDEO IMAGING SYSTEM
K972540 · Sopro · Sep 1997
OLYMPUS OES OTV-S5C VIDEO SYSTEM
K971416 · Olympus America, Inc. · Jul 1997
VISTA SINGLE CHIP VIDEO CAMERA
K971373 · Vista Medical Technologies, Inc. · May 1997