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 BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757

K-Number: K020523 · 2002-03-20

ApplicantBd
Decision Date2002-03-20
Product CodeSCL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757 is the device name listed in this FDA 510(k) record. The listed applicant is Bd. It received FDA 510(k) clearance on 2002-03-20 under 510(k) number K020523. The device is classified under product code SCL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757?

BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757 is a medical device that received FDA 510(k) clearance on 2002-03-20. The listed applicant is Bd. The 510(k) number is K020523.

When did BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757 receive FDA 510(k) clearance?

BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757 received FDA 510(k) clearance on 2002-03-20, under 510(k) number K020523.

Who is the listed applicant for BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757?

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

What is the FDA product code for BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757?

The FDA product code for BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757 is SCL.

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 Bd 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.

K253445BD Surgiphor™ 1000 mL Antimicrobial Irrigation System (910120)K240257Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery KitK232434BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived KitK223016BD VeritorTM System for Rapid Detection of Flu A+B CLIA-Waived KitK221504BD Surgiphor™ Antimicrobial Irrigation SystemK180438BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit

View all 15 devices →

Related Devices (Code: SCL)

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.

K250983Medblue Skin Prick Test Applicator (AS103, AS108, AS109, AS110, AS111, AS113, AS132, AS134, AS146, AS148, AS160, AS162, AS170, AS172)Asistan MedikalK222385Bifurcated NeedleAnhui Tiankang Medical Technology Co., Ltd.K182582Oryum and Ovem Epidermal Deri Prick Test ApplicatorAllergy & Applicator Depot, LLCK172062AllergiEnd ST-9 Multiple Skin Test Applicator, AllergiEnd ST-9 Multiple Well Test TrayMedscience Science Research Group, Inc.K162917Allerhope Allergy Skin TesterProcare Industrial Co., LimitedK032528BD ECLIPSE BIFURCATED NEEDLEBecton, Dickinson & CO

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.

↑