KSEA CLEARVISION LENS IRRIGATION SYSTEM
K-Number: K013838 · 2002-01-16
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Device Summary
Frequently Asked Questions
What is the KSEA CLEARVISION LENS IRRIGATION SYSTEM?
KSEA CLEARVISION LENS IRRIGATION SYSTEM is a medical device that received FDA 510(k) clearance on 2002-01-16. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K013838.
When did KSEA CLEARVISION LENS IRRIGATION SYSTEM receive FDA 510(k) clearance?
KSEA CLEARVISION LENS IRRIGATION SYSTEM received FDA 510(k) clearance on 2002-01-16, under 510(k) number K013838.
Who is the listed applicant for KSEA CLEARVISION LENS IRRIGATION 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 KSEA CLEARVISION LENS IRRIGATION SYSTEM?
The FDA product code for KSEA CLEARVISION LENS IRRIGATION SYSTEM is EOB.
Related Clinical Trials
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.
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: EOB)
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.
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