Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM)

K-Number: K023033 · 2002-11-26

Decision Date2002-11-26
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM) 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 2002-11-26 under 510(k) number K023033. 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 ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM)?

ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM) is a medical device that received FDA 510(k) clearance on 2002-11-26. The listed applicant is <Genx> Intl., Inc.. The 510(k) number is K023033.

When did ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM) receive FDA 510(k) clearance?

ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM) received FDA 510(k) clearance on 2002-11-26, under 510(k) number K023033.

Who is the listed applicant for ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM)?

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 ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM)?

The FDA product code for ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM) is MQL.

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.

Other records listing <Genx> Intl., 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 32 devices →

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.

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.

↑