VES 1501-M
K-Number: K982409 · 1998-08-21
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Device Summary
Frequently Asked Questions
What is the VES 1501-M?
VES 1501-M is a medical device that received FDA 510(k) clearance on 1998-08-21. The listed applicant is Angiolaz, Inc.. The 510(k) number is K982409.
When did VES 1501-M receive FDA 510(k) clearance?
VES 1501-M received FDA 510(k) clearance on 1998-08-21, under 510(k) number K982409.
Who is the listed applicant for VES 1501-M?
The FDA 510(k) record lists Angiolaz, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VES 1501-M?
The FDA product code for VES 1501-M is FWF.
Other records listing Angiolaz, 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: FWF)
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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