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FDA 510(k)

VIREX TB READY-TO-USE DSINFECTANT CLEANER & DEODORANT

K-Number: K964535 · 1996-12-13

Decision Date1996-12-13
Product CodeLRJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIREX TB READY-TO-USE DSINFECTANT CLEANER & DEODORANT is the device name listed in this FDA 510(k) record. The listed applicant is S.C. Johnson & Son, Inc.. It received FDA 510(k) clearance on 1996-12-13 under 510(k) number K964535. The device is classified under product code LRJ. It was reviewed by the HO advisory panel. Product code LRJ falls under the category of Clinical Lab, which includes general clinical laboratory instruments. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIREX TB READY-TO-USE DSINFECTANT CLEANER & DEODORANT?

VIREX TB READY-TO-USE DSINFECTANT CLEANER & DEODORANT is a medical device that received FDA 510(k) clearance on 1996-12-13. The listed applicant is S.C. Johnson & Son, Inc.. The 510(k) number is K964535.

When did VIREX TB READY-TO-USE DSINFECTANT CLEANER & DEODORANT receive FDA 510(k) clearance?

VIREX TB READY-TO-USE DSINFECTANT CLEANER & DEODORANT received FDA 510(k) clearance on 1996-12-13, under 510(k) number K964535.

Who is the listed applicant for VIREX TB READY-TO-USE DSINFECTANT CLEANER & DEODORANT?

The FDA 510(k) record lists S.C. Johnson & Son, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIREX TB READY-TO-USE DSINFECTANT CLEANER & DEODORANT?

The FDA product code for VIREX TB READY-TO-USE DSINFECTANT CLEANER & DEODORANT is LRJ. This falls under the Clinical Lab category.

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 S.C. Johnson & Son, 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.

Related Devices (Code: LRJ)

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

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