ENVISION ARTHROSCOPY VISUALIZATION SYSTEM
K-Number: K943666 · 1994-11-17
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Device Summary
Frequently Asked Questions
What is the ENVISION ARTHROSCOPY VISUALIZATION SYSTEM?
ENVISION ARTHROSCOPY VISUALIZATION SYSTEM is a medical device that received FDA 510(k) clearance on 1994-11-17. The listed applicant is Envision Surgical System, Inc.. The 510(k) number is K943666.
When did ENVISION ARTHROSCOPY VISUALIZATION SYSTEM receive FDA 510(k) clearance?
ENVISION ARTHROSCOPY VISUALIZATION SYSTEM received FDA 510(k) clearance on 1994-11-17, under 510(k) number K943666.
Who is the listed applicant for ENVISION ARTHROSCOPY VISUALIZATION SYSTEM?
The FDA 510(k) record lists Envision Surgical System, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENVISION ARTHROSCOPY VISUALIZATION SYSTEM?
The FDA product code for ENVISION ARTHROSCOPY VISUALIZATION SYSTEM is HRX.
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 Envision Surgical System, 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: HRX)
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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