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)

STORAGE, DIGITAL DSC-1, CONTROL UNIT

K-Number: K790288 · 1979-02-27

ApplicantOxford Medilog, Inc.
Decision Date1979-02-27
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STORAGE, DIGITAL DSC-1, CONTROL UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Medilog, Inc.. It received FDA 510(k) clearance on 1979-02-27 under 510(k) number K790288. 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 STORAGE, DIGITAL DSC-1, CONTROL UNIT?

STORAGE, DIGITAL DSC-1, CONTROL UNIT is a medical device that received FDA 510(k) clearance on 1979-02-27. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K790288.

When did STORAGE, DIGITAL DSC-1, CONTROL UNIT receive FDA 510(k) clearance?

STORAGE, DIGITAL DSC-1, CONTROL UNIT received FDA 510(k) clearance on 1979-02-27, under 510(k) number K790288.

Who is the listed applicant for STORAGE, DIGITAL DSC-1, CONTROL UNIT?

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

What is the FDA product code for STORAGE, DIGITAL DSC-1, CONTROL UNIT?

The FDA product code for STORAGE, DIGITAL DSC-1, CONTROL UNIT 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

Other records listing Oxford Medilog, 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.

K923737MODEL MEDILOG RAPIDEK920295MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED)K912890MODEL SONICAID AXISK912639SONICAID TEAMK904763MENTOR EEG SYSTEMK902690SONICAID MODEL MERIDIAN 800

View all 48 devices →

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.

↑