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FDA 510(k)

SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI

K-Number: K926013 · 1993-02-12

Decision Date1993-02-12
Product CodeLRJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI is the device name listed in this FDA 510(k) record. The listed applicant is Sporicidin Intl.. It received FDA 510(k) clearance on 1993-02-12 under 510(k) number K926013. 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 DISINFECT TOWEL, SPRAY/SOLUT MODI?

SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Sporicidin Intl.. The 510(k) number is K926013.

When did SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI receive FDA 510(k) clearance?

SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI received FDA 510(k) clearance on 1993-02-12, under 510(k) number K926013.

Who is the listed applicant for SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI?

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 DISINFECT TOWEL, SPRAY/SOLUT MODI?

The FDA product code for SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI 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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