VOX/BASE FOR WINDOWS
K-Number: K972933 · 1997-10-27
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Device Summary
Frequently Asked Questions
What is the VOX/BASE FOR WINDOWS?
VOX/BASE FOR WINDOWS is a medical device that received FDA 510(k) clearance on 1997-10-27. The listed applicant is J-Mac System, Inc.. The 510(k) number is K972933.
When did VOX/BASE FOR WINDOWS receive FDA 510(k) clearance?
VOX/BASE FOR WINDOWS received FDA 510(k) clearance on 1997-10-27, under 510(k) number K972933.
Who is the listed applicant for VOX/BASE FOR WINDOWS?
The FDA 510(k) record lists J-Mac System, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VOX/BASE FOR WINDOWS?
The FDA product code for VOX/BASE FOR WINDOWS is LLZ.
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.
Related Devices (Code: LLZ)
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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