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FDA 510(k)

GERITREX STERILE SALINE WET DRESSING

K-Number: K931510 · 1993-07-13

ApplicantGeritrex Corp.
Decision Date1993-07-13
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

GERITREX STERILE SALINE WET DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Geritrex Corp.. It received FDA 510(k) clearance on 1993-07-13 under 510(k) number K931510. 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 GERITREX STERILE SALINE WET DRESSING?

GERITREX STERILE SALINE WET DRESSING is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Geritrex Corp.. The 510(k) number is K931510.

When did GERITREX STERILE SALINE WET DRESSING receive FDA 510(k) clearance?

GERITREX STERILE SALINE WET DRESSING received FDA 510(k) clearance on 1993-07-13, under 510(k) number K931510.

Who is the listed applicant for GERITREX STERILE SALINE WET DRESSING?

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

What is the FDA product code for GERITREX STERILE SALINE WET DRESSING?

The FDA product code for GERITREX STERILE SALINE WET DRESSING 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 Geritrex Corp. 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.

K945224GRX FOAM DRESSINGK931509GERITREX STERILE SALINE SOLUTION FOR IRRIGATIONK931511GERITREX STERILE WATER FOR IRRIGATION

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.

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