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)

MIDA ALGORITHM REV. B

K-Number: K023414 · 2003-12-05

ApplicantOrtivus AB
Decision Date2003-12-05
Product CodeDYC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MIDA ALGORITHM REV. B is the device name listed in this FDA 510(k) record. The listed applicant is Ortivus AB. It received FDA 510(k) clearance on 2003-12-05 under 510(k) number K023414. The device is classified under product code DYC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDA ALGORITHM REV. B?

MIDA ALGORITHM REV. B is a medical device that received FDA 510(k) clearance on 2003-12-05. The listed applicant is Ortivus AB. The 510(k) number is K023414.

When did MIDA ALGORITHM REV. B receive FDA 510(k) clearance?

MIDA ALGORITHM REV. B received FDA 510(k) clearance on 2003-12-05, under 510(k) number K023414.

Who is the listed applicant for MIDA ALGORITHM REV. B?

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

What is the FDA product code for MIDA ALGORITHM REV. B?

The FDA product code for MIDA ALGORITHM REV. B is DYC.

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: DYC)

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.

K896396MIDA SYSTEM, MODELS 1000/1100Medical Graphics Corp.K823934CARIEL F12OdamK810529DIRECT WRITING VECTORCARDIOGRAPHElmed, 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.

↑