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FDA 510(k)

ACIDIFIED TYRODES SOLUTION

K-Number: K022547 · 2002-08-28

Applicant<Genx> Intl., Inc.
Decision Date2002-08-28
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ACIDIFIED TYRODES SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is <Genx> Intl., Inc.. It received FDA 510(k) clearance on 2002-08-28 under 510(k) number K022547. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACIDIFIED TYRODES SOLUTION?

ACIDIFIED TYRODES SOLUTION is a medical device that received FDA 510(k) clearance on 2002-08-28. The listed applicant is <Genx> Intl., Inc.. The 510(k) number is K022547.

When did ACIDIFIED TYRODES SOLUTION receive FDA 510(k) clearance?

ACIDIFIED TYRODES SOLUTION received FDA 510(k) clearance on 2002-08-28, under 510(k) number K022547.

Who is the listed applicant for ACIDIFIED TYRODES SOLUTION?

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

What is the FDA product code for ACIDIFIED TYRODES SOLUTION?

The FDA product code for ACIDIFIED TYRODES SOLUTION is MQL.

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Related Devices (Code: MQL)

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.

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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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