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FDA 510(k)

HY-CHLO(TM)WOUND SCRUB

K-Number: K113312 · 2012-08-21

ApplicantPatrin Pharma
Decision Date2012-08-21
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HY-CHLO(TM)WOUND SCRUB is the device name listed in this FDA 510(k) record. The listed applicant is Patrin Pharma. It received FDA 510(k) clearance on 2012-08-21 under 510(k) number K113312. 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 HY-CHLO(TM)WOUND SCRUB?

HY-CHLO(TM)WOUND SCRUB is a medical device that received FDA 510(k) clearance on 2012-08-21. The listed applicant is Patrin Pharma. The 510(k) number is K113312.

When did HY-CHLO(TM)WOUND SCRUB receive FDA 510(k) clearance?

HY-CHLO(TM)WOUND SCRUB received FDA 510(k) clearance on 2012-08-21, under 510(k) number K113312.

Who is the listed applicant for HY-CHLO(TM)WOUND SCRUB?

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

What is the FDA product code for HY-CHLO(TM)WOUND SCRUB?

The FDA product code for HY-CHLO(TM)WOUND SCRUB is FQH.

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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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