KARL STORZ ICG Imaging System
K-Number: K171238 · 2017-05-25
Device Summary
Frequently Asked Questions
What is the KARL STORZ ICG Imaging System?
KARL STORZ ICG Imaging System is a medical device that received FDA 510(k) clearance on 2017-05-25. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K171238.
When did KARL STORZ ICG Imaging System receive FDA 510(k) clearance?
KARL STORZ ICG Imaging System received FDA 510(k) clearance on 2017-05-25, under 510(k) number K171238.
Who is the listed applicant for KARL STORZ ICG Imaging System?
The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KARL STORZ ICG Imaging System?
The FDA product code for KARL STORZ ICG Imaging System is OWN.
Other records listing KARL STORZ Endoscopy-America, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OWN)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.