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)

EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088

K-Number: K011941 · 2001-08-22

ApplicantThe Kendall Company
Decision Date2001-08-22
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088 is the device name listed in this FDA 510(k) record. The listed applicant is The Kendall Company. It received FDA 510(k) clearance on 2001-08-22 under 510(k) number K011941. 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 EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088?

EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088 is a medical device that received FDA 510(k) clearance on 2001-08-22. The listed applicant is The Kendall Company. The 510(k) number is K011941.

When did EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088 receive FDA 510(k) clearance?

EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088 received FDA 510(k) clearance on 2001-08-22, under 510(k) number K011941.

Who is the listed applicant for EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088?

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

What is the FDA product code for EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088?

The FDA product code for EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088 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 The Kendall Company 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.

K061936KENDALL ARGYLE NEONATAL/PEDIATRIC PICC, MODEL 43311K030209MAHURKAR OPLUS CATHETER, MODEL 13.5 FRK020089MAHURKAR TRIPLE LUMEN CATHETER, 12 FRK011283MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGEK002902TANDEM-CATH 10 FR. CATHETER SYSTEM, MODEL MULTIPLE CODE NUMBERSK002901KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER

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.

↑