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FDA 510(k)

VD ALERT

K-Number: K820520 · 1982-05-14

ApplicantIntl. Research Distributors, Inc.
Decision Date1982-05-14
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VD ALERT is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Research Distributors, Inc.. It received FDA 510(k) clearance on 1982-05-14 under 510(k) number K820520. The device is classified under product code LIO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VD ALERT?

VD ALERT is a medical device that received FDA 510(k) clearance on 1982-05-14. The listed applicant is Intl. Research Distributors, Inc.. The 510(k) number is K820520.

When did VD ALERT receive FDA 510(k) clearance?

VD ALERT received FDA 510(k) clearance on 1982-05-14, under 510(k) number K820520.

Who is the listed applicant for VD ALERT?

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

What is the FDA product code for VD ALERT?

The FDA product code for VD ALERT is LIO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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