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FDA 510(k)

MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION

K-Number: K003087 · 2000-11-07

Decision Date2000-11-07
Product CodeMED
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Sporicidin Intl.. It received FDA 510(k) clearance on 2000-11-07 under 510(k) number K003087. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION?

MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION is a medical device that received FDA 510(k) clearance on 2000-11-07. The listed applicant is Sporicidin Intl.. The 510(k) number is K003087.

When did MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION receive FDA 510(k) clearance?

MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION received FDA 510(k) clearance on 2000-11-07, under 510(k) number K003087.

Who is the listed applicant for MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION?

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 MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION?

The FDA product code for MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION is MED.

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: MED)

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.

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