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)

IPAG MICRONOVA INTERFACE #781111

K-Number: K791753 · 1979-10-02

ApplicantRobinton Corp.
Decision Date1979-10-02
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IPAG MICRONOVA INTERFACE #781111 is the device name listed in this FDA 510(k) record. The listed applicant is Robinton Corp.. It received FDA 510(k) clearance on 1979-10-02 under 510(k) number K791753. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPAG MICRONOVA INTERFACE #781111?

IPAG MICRONOVA INTERFACE #781111 is a medical device that received FDA 510(k) clearance on 1979-10-02. The listed applicant is Robinton Corp.. The 510(k) number is K791753.

When did IPAG MICRONOVA INTERFACE #781111 receive FDA 510(k) clearance?

IPAG MICRONOVA INTERFACE #781111 received FDA 510(k) clearance on 1979-10-02, under 510(k) number K791753.

Who is the listed applicant for IPAG MICRONOVA INTERFACE #781111?

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

What is the FDA product code for IPAG MICRONOVA INTERFACE #781111?

The FDA product code for IPAG MICRONOVA INTERFACE #781111 is DXG.

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

Related Devices (Code: DXG)

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.

K253092Argos Infinity (Rev. 1.0)Retia Medical Systems, Inc.K251275VitalStream ART Connect; VitalStream-HemoCaretaker MedicalK232048Cogent™ Hemodynamic Monitoring System; Cogent™ HMSIcu MedicalK212529Hypotension Decision Assist Model HDA-OR2Directed Systems, Ltd.K192169PulsioFlex Monitoring System with ProAQT SensorPulsion Medical Systems SEK193179EV1000 Clinical PlatformEdwards Lifesciences, LLC

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.

↑