PAX-500
K-Number: K082350 · 2008-10-10
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Device Summary
Frequently Asked Questions
What is the PAX-500?
PAX-500 is a medical device that received FDA 510(k) clearance on 2008-10-10. The listed applicant is VATECH Co., Ltd.. The 510(k) number is K082350.
When did PAX-500 receive FDA 510(k) clearance?
PAX-500 received FDA 510(k) clearance on 2008-10-10, under 510(k) number K082350.
Who is the listed applicant for PAX-500?
The FDA 510(k) record lists VATECH Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PAX-500?
The FDA product code for PAX-500 is OAS.
Other records listing VATECH Co., Ltd. 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: OAS)
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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