KARL STORZ ICG Imaging System

FDA 510(k) K171238 · KARL STORZ Endoscopy-America, Inc.

Substantially Equivalent

510(k) numberK171238

Submission

Device name
KARL STORZ ICG Imaging System
Applicant
KARL STORZ Endoscopy-America, Inc.
El Segundo, CA, US
Received
April 27, 2017
Decision date
May 25, 2017
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OWN – Confocal Optical Imaging
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

Collection of light signals for visualization of cellular microstructures.

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Questions and answers

When was KARL STORZ ICG Imaging System cleared by the FDA?

KARL STORZ ICG Imaging System (K171238) received a 510(k) decision of Substantially Equivalent on May 25, 2017, 28 days after the submission was received.

What is the product code of K171238?

The FDA product code is OWN – Confocal Optical Imaging, a Class II (moderate risk) device regulated under 21 CFR 876.1500.