VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM
K-Number: K982397 · 1998-09-10
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Device Summary
Frequently Asked Questions
What is the VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM?
VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM is a medical device that received FDA 510(k) clearance on 1998-09-10. The listed applicant is Angiolaz, Inc.. The 510(k) number is K982397.
When did VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM receive FDA 510(k) clearance?
VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM received FDA 510(k) clearance on 1998-09-10, under 510(k) number K982397.
Who is the listed applicant for VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM?
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 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM?
The FDA product code for VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM is FWF.
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 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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