KSEA QUADRO SWITCH
K-Number: K021776 · 2002-08-15
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Device Summary
Frequently Asked Questions
What is the KSEA QUADRO SWITCH?
KSEA QUADRO SWITCH is a medical device that received FDA 510(k) clearance on 2002-08-15. The listed applicant is Karl Storz Endoscopy. The 510(k) number is K021776.
When did KSEA QUADRO SWITCH receive FDA 510(k) clearance?
KSEA QUADRO SWITCH received FDA 510(k) clearance on 2002-08-15, under 510(k) number K021776.
Who is the listed applicant for KSEA QUADRO SWITCH?
The FDA 510(k) record lists Karl Storz Endoscopy as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KSEA QUADRO SWITCH?
The FDA product code for KSEA QUADRO SWITCH is OCX.
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 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: OCX)
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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