Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BD Vaginal Panel

K-Number: K223653 · 2023-03-06

ApplicantBecton, Dickinson and Company
Decision Date2023-03-06
Product CodePQA
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BD Vaginal Panel is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2023-03-06 under approval number K223653. The device is classified under product code PQA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD Vaginal Panel?

BD Vaginal Panel is a medical device that received FDA 510(k) clearance on 2023-03-06. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K223653.

When was BD Vaginal Panel approved by the FDA?

BD Vaginal Panel received FDA 510(k) clearance on 2023-03-06, under approval number K223653.

What company makes BD Vaginal Panel?

BD Vaginal Panel is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Vaginal Panel?

The FDA product code for BD Vaginal Panel is PQA.

Other Devices by Becton, Dickinson and Company

K162081BD 1ml Luer-lok Hypodermic Syringe, BD 1 mL Luer-Lok Hypodermic Syringe with BD Hypodermic Needle or BD Eclipse Hypodermic Needle, BD 1ml Luer-lok Insulin Syringe K162516BD Pen Needle K160657BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube K151589BD MAX CT/GC/TV, BD MAX INSTRUMENT K151870BD U-500 INSULIN SYRINGE K161553BD SafeAssist

View all 100 devices →

Related Devices (Code: PQA)

DEN160001BD MAX Vaginal Panel, BD MAX InstrumentGeneohm Sciences Canada, Inc. (Bd Diagnostics) K191957BD MAX Vaginal PanelGeneohm Sciences Canada, Inc. (Bd Diagnostics) K190452Aptima BV AssayHologic, Inc. K190472Aptima CV/TV AssayHologic, Inc. K201017BD MAX Vaginal Panel, BD MAX System, BD Molecular Swab Collection KitGeneohm Sciences Canada, Inc. (Bd Life Sciences) K221160Xpert Xpress MVP, GeneXpert Dx System, GeneXpert Infinity SystemCepheid

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.

↑