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)

MODEL MEDILOG RAPIDE

K-Number: K923737 · 1994-01-05

ApplicantOxford Medilog, Inc.
Decision Date1994-01-05
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL MEDILOG RAPIDE 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 1994-01-05 under 510(k) number K923737. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL MEDILOG RAPIDE?

MODEL MEDILOG RAPIDE is a medical device that received FDA 510(k) clearance on 1994-01-05. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K923737.

When did MODEL MEDILOG RAPIDE receive FDA 510(k) clearance?

MODEL MEDILOG RAPIDE received FDA 510(k) clearance on 1994-01-05, under 510(k) number K923737.

Who is the listed applicant for MODEL MEDILOG RAPIDE?

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 MODEL MEDILOG RAPIDE?

The FDA product code for MODEL MEDILOG RAPIDE is BZQ.

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.

K920295MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED)K912890MODEL SONICAID AXISK912639SONICAID TEAMK904763MENTOR EEG SYSTEMK902690SONICAID MODEL MERIDIAN 800K895909SONICAID MODEL VASOFLO 4

View all 48 devices →

Related Devices (Code: BZQ)

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.

K253274BedDot (G1)Intelligent Dots, LLCK251326Respiration Rate algorithmEdwards Lifesciences, LLCK250093Linshom Continuous Predictive Respiratory Monitoring System (CPRMS)Linshom Medical, Inc.K250934Respiree Cardio- Respiratory Monitor SystemRespiree Pte, Ltd.K243183RTMsense Respiratory Monitoring SystemRtm Vital Signs, LLCK243966FaceHeart Vitals Software Development Kit (FH vitals SDK-RR)Faceheart Corp.

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.

↑