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)

MINATURE PRESSURE TRANSDUCER

K-Number: K834040 · 1984-02-10

ApplicantCarbomedics, Inc.
Decision Date1984-02-10
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINATURE PRESSURE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Carbomedics, Inc.. It received FDA 510(k) clearance on 1984-02-10 under 510(k) number K834040. 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 MINATURE PRESSURE TRANSDUCER?

MINATURE PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is Carbomedics, Inc.. The 510(k) number is K834040.

When did MINATURE PRESSURE TRANSDUCER receive FDA 510(k) clearance?

MINATURE PRESSURE TRANSDUCER received FDA 510(k) clearance on 1984-02-10, under 510(k) number K834040.

Who is the listed applicant for MINATURE PRESSURE TRANSDUCER?

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

What is the FDA product code for MINATURE PRESSURE TRANSDUCER?

The FDA product code for MINATURE PRESSURE TRANSDUCER 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 Carbomedics, 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.

K970375ANNULOFLO SYSTEMK964665VASCUTEK GELWEAVE VASCULAR GRAFT (BIFURCATED CONFIGURATION)K962154CARBOMEDICS HANDLEK960923CARBOMEDICS MITRAL ROTATORK960706VASCUTEK VASCUSOFT PLUS VASCULAR GRAFTK960169CARBOMEDICS VALVE TESTER

View all 22 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.

↑