OCULUS PURACYN ANTIMICROBIAL SKIN AND WOUND CLEANSER
K-Number: K090206 · 2009-06-02
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Device Summary
Frequently Asked Questions
What is the OCULUS PURACYN ANTIMICROBIAL SKIN AND WOUND CLEANSER?
OCULUS PURACYN ANTIMICROBIAL SKIN AND WOUND CLEANSER is a medical device that received FDA 510(k) clearance on 2009-06-02. The listed applicant is Oculus Innovative Sciences, Inc.. The 510(k) number is K090206.
When did OCULUS PURACYN ANTIMICROBIAL SKIN AND WOUND CLEANSER receive FDA 510(k) clearance?
OCULUS PURACYN ANTIMICROBIAL SKIN AND WOUND CLEANSER received FDA 510(k) clearance on 2009-06-02, under 510(k) number K090206.
Who is the listed applicant for OCULUS PURACYN ANTIMICROBIAL SKIN AND WOUND CLEANSER?
The FDA 510(k) record lists Oculus Innovative Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OCULUS PURACYN ANTIMICROBIAL SKIN AND WOUND CLEANSER?
The FDA product code for OCULUS PURACYN ANTIMICROBIAL SKIN AND WOUND CLEANSER is FRO. This falls under the Anesthesiology 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 Oculus Innovative Sciences, Inc. 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: FRO)
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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