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)

VASHE SKIN AND WOUND HYDROGEL

K-Number: K123071 · 2013-01-24

ApplicantPuricore, Inc.
Decision Date2013-01-24
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

VASHE SKIN AND WOUND HYDROGEL is the device name listed in this FDA 510(k) record. The listed applicant is Puricore, Inc.. It received FDA 510(k) clearance on 2013-01-24 under 510(k) number K123071. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASHE SKIN AND WOUND HYDROGEL?

VASHE SKIN AND WOUND HYDROGEL is a medical device that received FDA 510(k) clearance on 2013-01-24. The listed applicant is Puricore, Inc.. The 510(k) number is K123071.

When did VASHE SKIN AND WOUND HYDROGEL receive FDA 510(k) clearance?

VASHE SKIN AND WOUND HYDROGEL received FDA 510(k) clearance on 2013-01-24, under 510(k) number K123071.

Who is the listed applicant for VASHE SKIN AND WOUND HYDROGEL?

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

What is the FDA product code for VASHE SKIN AND WOUND HYDROGEL?

The FDA product code for VASHE SKIN AND WOUND HYDROGEL 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Puricore, 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.

K123072VASHE WOUND THERAPY SOLUTIONK100918VASHE WOUND THERAPY SYSTEM MODEL: 9000-0014K093697VASHE WOUND THERAPY SOLUTIONK093155VASHE WOUND CLEANSING SYSTEMK092232MODIFICATION TO:VASHE WOUND CLEANSING SYSTEM, MODEL 9000-0014K063159STERILOX LIQUID CHEMICAL STERILANT SYSTEM

View all 8 devices →

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.

K254168Actolind® (06.3637. Actolind® Gel Plus)ACTO GmbHK254041SkinSmart Antimicrobial HydroGelMagic Science Supply, LLCK261646Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd.K253665Vashe Plus Antimicrobial SolutionUrgo Medical North America, LLCK251929SilverCeuticals® Antimicrobial Wound GelSilverceuticals, Inc.K261023Microdacyn Wound Irrigation SolutionSonoma Pharmaceuticals, Inc.

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.

↑