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FDA 510(k)

VG-A MIG

K-Number: K924229 · 1992-11-27

Decision Date1992-11-27
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VG-A MIG is the device name listed in this FDA 510(k) record. The listed applicant is Vortech Data, Inc.. It received FDA 510(k) clearance on 1992-11-27 under 510(k) number K924229. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VG-A MIG?

VG-A MIG is a medical device that received FDA 510(k) clearance on 1992-11-27. The listed applicant is Vortech Data, Inc.. The 510(k) number is K924229.

When did VG-A MIG receive FDA 510(k) clearance?

VG-A MIG received FDA 510(k) clearance on 1992-11-27, under 510(k) number K924229.

Who is the listed applicant for VG-A MIG?

The FDA 510(k) record lists Vortech Data, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VG-A MIG?

The FDA product code for VG-A MIG is LMD.

Other records listing Vortech Data, 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.

View all 11 devices →

Related Devices (Code: LMD)

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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