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)

SAFEDWEEL DRESSING CHANGE TRAY

K-Number: K950438 · 1995-03-15

ApplicantBecton Dickinson Vascular Access, Inc.
Decision Date1995-03-15
Product CodeFRG
Advisory CommitteeHO
DecisionUnknown

Device Summary

SAFEDWEEL DRESSING CHANGE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Vascular Access, Inc.. It received FDA 510(k) clearance on 1995-03-15 under 510(k) number K950438. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SAFEDWEEL DRESSING CHANGE TRAY?

SAFEDWEEL DRESSING CHANGE TRAY is a medical device that received FDA 510(k) clearance on 1995-03-15. The listed applicant is Becton Dickinson Vascular Access, Inc.. The 510(k) number is K950438.

When did SAFEDWEEL DRESSING CHANGE TRAY receive FDA 510(k) clearance?

SAFEDWEEL DRESSING CHANGE TRAY received FDA 510(k) clearance on 1995-03-15, under 510(k) number K950438.

Who is the listed applicant for SAFEDWEEL DRESSING CHANGE TRAY?

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

What is the FDA product code for SAFEDWEEL DRESSING CHANGE TRAY?

The FDA product code for SAFEDWEEL 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_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 Becton Dickinson Vascular Access, 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.

K971339INSYTE, INSYTE-W, INSYTE AUTOGUARD CATHETERSK970259E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SETK964049FIRST MIDCATH CATHETER WITH DUAL LUMENSK964050FIRST MIDCATH CATHETERK964048FIRST MIDCATH CATHETER KITK954906FIRST PICC INTRODUCER CATHETER

View all 25 devices →

Related Devices (Code: FRG)

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.

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, LLCK253454HALYARD* 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.

↑