SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI
K-Number: K926013 · 1993-02-12
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Device Summary
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.
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
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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