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FDA 510(k)

SPORICIDIN BRAND DISINFECTANT TOWELETTES

K-Number: K904579 · 1992-05-18

Decision Date1992-05-18
Product CodeLRJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPORICIDIN BRAND DISINFECTANT TOWELETTES is the device name listed in this FDA 510(k) record. The listed applicant is Sporicidin Intl.. It received FDA 510(k) clearance on 1992-05-18 under 510(k) number K904579. 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 SPORICIDIN BRAND DISINFECTANT TOWELETTES?

SPORICIDIN BRAND DISINFECTANT TOWELETTES is a medical device that received FDA 510(k) clearance on 1992-05-18. The listed applicant is Sporicidin Intl.. The 510(k) number is K904579.

When did SPORICIDIN BRAND DISINFECTANT TOWELETTES receive FDA 510(k) clearance?

SPORICIDIN BRAND DISINFECTANT TOWELETTES received FDA 510(k) clearance on 1992-05-18, under 510(k) number K904579.

Who is the listed applicant for SPORICIDIN BRAND DISINFECTANT TOWELETTES?

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

What is the FDA product code for SPORICIDIN BRAND DISINFECTANT TOWELETTES?

The FDA product code for SPORICIDIN BRAND DISINFECTANT TOWELETTES 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 Sporicidin Intl. 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 8 devices →

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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