KSEA OPSERVER LAP
K-Number: K031895 · 2003-09-23
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Device Summary
Frequently Asked Questions
What is the KSEA OPSERVER LAP?
KSEA OPSERVER LAP is a medical device that received FDA 510(k) clearance on 2003-09-23. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K031895.
When did KSEA OPSERVER LAP receive FDA 510(k) clearance?
KSEA OPSERVER LAP received FDA 510(k) clearance on 2003-09-23, under 510(k) number K031895.
Who is the listed applicant for KSEA OPSERVER LAP?
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 OPSERVER LAP?
The FDA product code for KSEA OPSERVER LAP is FET.
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: FET)
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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