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FDA 510(k)

VOX/BASE FOR WINDOWS

K-Number: K972933 · 1997-10-27

Decision Date1997-10-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VOX/BASE FOR WINDOWS is the device name listed in this FDA 510(k) record. The listed applicant is J-Mac System, Inc.. It received FDA 510(k) clearance on 1997-10-27 under 510(k) number K972933. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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

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