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)

BD PureHub Disinfecting Cap

K-Number: K193190 · 2020-11-09

ApplicantBecton, Dickinson and Company
Decision Date2020-11-09
Product CodeQBP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD PureHub Disinfecting Cap is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2020-11-09 under 510(k) number K193190. The device is classified under product code QBP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD PureHub Disinfecting Cap?

BD PureHub Disinfecting Cap is a medical device that received FDA 510(k) clearance on 2020-11-09. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K193190.

When did BD PureHub Disinfecting Cap receive FDA 510(k) clearance?

BD PureHub Disinfecting Cap received FDA 510(k) clearance on 2020-11-09, under 510(k) number K193190.

Who is the listed applicant for BD PureHub Disinfecting Cap?

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

What is the FDA product code for BD PureHub Disinfecting Cap?

The FDA product code for BD PureHub Disinfecting Cap is QBP.

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.

NCT05957406SMART TRENDS StudyCOMPLETEDNCT06492746Personal BP - CAI StudyRECRUITINGNCT07148323HemoSphere Alta StudyRECRUITINGNCT07216573The Continuity StudyRECRUITINGNCT07317648ClearSight NextGen1 StudyCOMPLETED

Other records listing Becton, Dickinson and 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.

PMA P160037KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUSK260128BD Preset™ and BD A-Line™ Arterial Blood Collection SyringesK252506BD Vacutainer® Safety-Lok™ Blood Collection Set; BD Vacutainer® Safety-Lok™ Blood Collection Set with Pre-Attached HolderK252378BD® MiniDraw™ Capillary Blood Collection System with BD® MiniDraw™ SST™ Capillary Blood Collection TubeK260184Onclarity™ Self-Collection KitK252040BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes

View all 100 devices →

Related Devices (Code: QBP)

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.

K252006OTTO™ Disinfecting CapIcu Medical, Inc.K251592SteriHub™ Disinfecting Device and Protective Cover1World Vista MedicalK223914ACTIV™ CapCleansite Medical, Inc.K200299Curos Jet Disinfecting Cap3M CompanyK192382CapKlenZStar Mountain Medical, Inc.K190918SwabTip Male Disinfectant CapIcu Medical

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.

↑