HPR PLUS EMOLLIENT FOAM
K-Number: K113774 · 2012-02-09
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Device Summary
Frequently Asked Questions
What is the HPR PLUS EMOLLIENT FOAM?
HPR PLUS EMOLLIENT FOAM is a medical device that received FDA 510(k) clearance on 2012-02-09. The listed applicant is Prugen IP Holdings, Inc.. The 510(k) number is K113774.
When did HPR PLUS EMOLLIENT FOAM receive FDA 510(k) clearance?
HPR PLUS EMOLLIENT FOAM received FDA 510(k) clearance on 2012-02-09, under 510(k) number K113774.
Who is the listed applicant for HPR PLUS EMOLLIENT FOAM?
The FDA 510(k) record lists Prugen IP Holdings, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HPR PLUS EMOLLIENT FOAM?
The FDA product code for HPR PLUS EMOLLIENT FOAM 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 Prugen IP Holdings, 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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