Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EXSEPT SKIN AND WOUND CLEANSER WITH ANTIMICROBIAL PRESERVATIVE

K-Number: K111313 · 2011-12-14

Decision Date2011-12-14
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXSEPT SKIN AND WOUND CLEANSER WITH ANTIMICROBIAL PRESERVATIVE is the device name listed in this FDA 510(k) record. The listed applicant is Alcavis Hdc, LLC. It received FDA 510(k) clearance on 2011-12-14 under 510(k) number K111313. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXSEPT SKIN AND WOUND CLEANSER WITH ANTIMICROBIAL PRESERVATIVE?

EXSEPT SKIN AND WOUND CLEANSER WITH ANTIMICROBIAL PRESERVATIVE is a medical device that received FDA 510(k) clearance on 2011-12-14. The listed applicant is Alcavis Hdc, LLC. The 510(k) number is K111313.

When did EXSEPT SKIN AND WOUND CLEANSER WITH ANTIMICROBIAL PRESERVATIVE receive FDA 510(k) clearance?

EXSEPT SKIN AND WOUND CLEANSER WITH ANTIMICROBIAL PRESERVATIVE received FDA 510(k) clearance on 2011-12-14, under 510(k) number K111313.

Who is the listed applicant for EXSEPT SKIN AND WOUND CLEANSER WITH ANTIMICROBIAL PRESERVATIVE?

The FDA 510(k) record lists Alcavis Hdc, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXSEPT SKIN AND WOUND CLEANSER WITH ANTIMICROBIAL PRESERVATIVE?

The FDA product code for EXSEPT SKIN AND WOUND CLEANSER WITH ANTIMICROBIAL PRESERVATIVE is FQH.

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.

Related Devices (Code: FQH)

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.

↑