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)

MILLEX VV, GV, AND HV SYRINGE FILTER UNITS

K-Number: K023892 · 2003-01-17

ApplicantMillipore Corp.
Decision Date2003-01-17
Product CodeBSN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MILLEX VV, GV, AND HV SYRINGE FILTER UNITS is the device name listed in this FDA 510(k) record. The listed applicant is Millipore Corp.. It received FDA 510(k) clearance on 2003-01-17 under 510(k) number K023892. The device is classified under product code BSN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLEX VV, GV, AND HV SYRINGE FILTER UNITS?

MILLEX VV, GV, AND HV SYRINGE FILTER UNITS is a medical device that received FDA 510(k) clearance on 2003-01-17. The listed applicant is Millipore Corp.. The 510(k) number is K023892.

When did MILLEX VV, GV, AND HV SYRINGE FILTER UNITS receive FDA 510(k) clearance?

MILLEX VV, GV, AND HV SYRINGE FILTER UNITS received FDA 510(k) clearance on 2003-01-17, under 510(k) number K023892.

Who is the listed applicant for MILLEX VV, GV, AND HV SYRINGE FILTER UNITS?

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

What is the FDA product code for MILLEX VV, GV, AND HV SYRINGE FILTER UNITS?

The FDA product code for MILLEX VV, GV, AND HV SYRINGE FILTER UNITS is BSN.

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 Millipore Corp. 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.

K013988MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 RK963717MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)K941326ULTRAFREE-CLK934069MILLEX, DUALEX (PLUS, ULTRA)K924347WATERS(TM) 996 PDAK922388WATERS(TM) LC MODULE I FOR CLINICAL USE

View all 30 devices →

Related Devices (Code: BSN)

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.

K190663Epidural MiniFilter LUER 80369-7, Epidural MiniFilter NRFit 80369-6PAJUNK GmbH MedizintechnologieK083451PORTEX EPIDURAL FILTER, MODEL 100/386/010, VARIOUS STANDARD AND CUSTOM TRAYSSmiths Medical Asd, Inc.K013988MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 RMillipore Corp.K963717MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)Millipore Corp.K960928SYRINGEFILTERArbor Technologies, Inc.K902666ANESTHESIA CONDUCTION FILTERArbor Technologies, 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.

↑