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)

INNERSENSE(TM) DISPOSABLE MICROTRANSDUCER

K-Number: K924737 · 1993-08-23

ApplicantBecton Dickinson Vascular Access, Inc.
Decision Date1993-08-23
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INNERSENSE(TM) DISPOSABLE MICROTRANSDUCER 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 1993-08-23 under 510(k) number K924737. The device is classified under product code DXO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INNERSENSE(TM) DISPOSABLE MICROTRANSDUCER?

INNERSENSE(TM) DISPOSABLE MICROTRANSDUCER is a medical device that received FDA 510(k) clearance on 1993-08-23. The listed applicant is Becton Dickinson Vascular Access, Inc.. The 510(k) number is K924737.

When did INNERSENSE(TM) DISPOSABLE MICROTRANSDUCER receive FDA 510(k) clearance?

INNERSENSE(TM) DISPOSABLE MICROTRANSDUCER received FDA 510(k) clearance on 1993-08-23, under 510(k) number K924737.

Who is the listed applicant for INNERSENSE(TM) DISPOSABLE MICROTRANSDUCER?

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 INNERSENSE(TM) DISPOSABLE MICROTRANSDUCER?

The FDA product code for INNERSENSE(TM) DISPOSABLE MICROTRANSDUCER is DXO.

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 SETK964048FIRST MIDCATH CATHETER KITK964050FIRST MIDCATH CATHETERK964049FIRST MIDCATH CATHETER WITH DUAL LUMENSK954906FIRST PICC INTRODUCER CATHETER

View all 25 devices →

Related Devices (Code: DXO)

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.

K251367OptoMonitor 3Opsens, Inc.K241418OptoMonitor 3Opsens, Inc.K233904ACIST RXi System (016616); ACIST Navvus II Catheter (016675_Acist Medical Systems, Inc.K222216TruWave Disposable Pressure TransducerEdwards Lifesciences, LLCK202943OptoMonitor 3Opsens, Inc.K193620OptoMonitor 3Opsens, 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.

↑