FDA 510(k)

JJ SKINNER CAREKITS WOUND CARE MANAGEMENT/DRESSING CHANGE TRAY

K-Number: K961227 · 1996-06-10

Decision Date1996-06-10

Product CodeFRG

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

JJ SKINNER CAREKITS WOUND CARE MANAGEMENT/DRESSING CHANGE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is J.J. Skinner, Inc.. It received FDA 510(k) clearance on 1996-06-10 under 510(k) number K961227. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JJ SKINNER CAREKITS WOUND CARE MANAGEMENT/DRESSING CHANGE TRAY?

JJ SKINNER CAREKITS WOUND CARE MANAGEMENT/DRESSING CHANGE TRAY is a medical device that received FDA 510(k) clearance on 1996-06-10. The listed applicant is J.J. Skinner, Inc.. The 510(k) number is K961227.

When did JJ SKINNER CAREKITS WOUND CARE MANAGEMENT/DRESSING CHANGE TRAY receive FDA 510(k) clearance?

JJ SKINNER CAREKITS WOUND CARE MANAGEMENT/DRESSING CHANGE TRAY received FDA 510(k) clearance on 1996-06-10, under 510(k) number K961227.

Who is the listed applicant for JJ SKINNER CAREKITS WOUND CARE MANAGEMENT/DRESSING CHANGE TRAY?

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

What is the FDA product code for JJ SKINNER CAREKITS WOUND CARE MANAGEMENT/DRESSING CHANGE TRAY?

The FDA product code for JJ SKINNER CAREKITS WOUND CARE MANAGEMENT/DRESSING CHANGE TRAY is FRG.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing J.J. Skinner, Inc. as applicant

K961683JJ SKINNER CAREKITS MINOR SURGICAL PROCEDURE TRAY K925469JJ SKINNER CAREKITS(TM) DIALYSIS ON/OFF KIT K925467JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KIT K925468JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KIT K903545CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITS K903544CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS

View all 7 devices →

Related Devices (Code: FRG)

K261897HALYARD* ARMOR-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* HEAVY-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* STANDARD-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD* H300W Sterilization Wrap with ASSURE-DRY* TechnologyO&M Halyard, Inc.K252823Dukal Crepe Paper Sterilization WrapDukal, LLC K253454HALYARD* ONE-STEP* Sterilization Wrap; HALYARD* QUICK CHECK* Sterilization Wrap; HALYARD* SEQUENTIAL Sterilization Wrap; HALYARD* SMART-FOLD* Sterilization WrapO&M Halyard, Inc.K251347Sterilization Pouch/RollSterivic Medical Co., Ltd.K251177Self-Seal Sterilization Pouch and RollGuangdong Maidi Medical Co., Ltd.K250306Chex-All Sterilization Pouches and TubesPropper Manufacturing Co., 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.