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)

MEDIRESP III

K-Number: K924272 · 1994-02-09

ApplicantMedflow Corp., Inc.
Decision Date1994-02-09
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDIRESP III is the device name listed in this FDA 510(k) record. The listed applicant is Medflow Corp., Inc.. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K924272. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIRESP III?

MEDIRESP III is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Medflow Corp., Inc.. The 510(k) number is K924272.

When did MEDIRESP III receive FDA 510(k) clearance?

MEDIRESP III received FDA 510(k) clearance on 1994-02-09, under 510(k) number K924272.

Who is the listed applicant for MEDIRESP III?

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

What is the FDA product code for MEDIRESP III?

The FDA product code for MEDIRESP III is BTL.

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: BTL)

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.

K242769VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031)Draegerwerk AG & CO KgaaK221634Oxymag - Transport and Emergency VentilatorMagnamed Tecnologia Medica S/AK202219VORTRAN GO2VENT with PEEP ValveVortran Medical Technology 1, Inc.K193191MEDUMAT Easy CPR, MEDUMAT Easy CPR with bagWeinmann Emergency Medical Technology GmbH + Co. KGK182956Puffin Lite Infant Resuscitation SystemInternational BiomedicalK173373SafeT T-Piece ResuscitatorVentlab, 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.

↑