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)

MEDIX ELECTRONIC NEBULIZING SYSTEM

K-Number: K853071 · 1985-08-29

ApplicantMedix Corp.
Decision Date1985-08-29
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDIX ELECTRONIC NEBULIZING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medix Corp.. It received FDA 510(k) clearance on 1985-08-29 under 510(k) number K853071. The device is classified under product code CCQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIX ELECTRONIC NEBULIZING SYSTEM?

MEDIX ELECTRONIC NEBULIZING SYSTEM is a medical device that received FDA 510(k) clearance on 1985-08-29. The listed applicant is Medix Corp.. The 510(k) number is K853071.

When did MEDIX ELECTRONIC NEBULIZING SYSTEM receive FDA 510(k) clearance?

MEDIX ELECTRONIC NEBULIZING SYSTEM received FDA 510(k) clearance on 1985-08-29, under 510(k) number K853071.

Who is the listed applicant for MEDIX ELECTRONIC NEBULIZING SYSTEM?

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

What is the FDA product code for MEDIX ELECTRONIC NEBULIZING SYSTEM?

The FDA product code for MEDIX ELECTRONIC NEBULIZING SYSTEM is CCQ.

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 Medix Corp. 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.

K921273EASIMIST ULTRASONIC NEBULIZERK914772MEDIX NEBULIZING SYSTEM CODE NO. 2000 AND 2001K822454SYRINGE PUMP 209-100K780444NERVTRON-RX

Related Devices (Code: CCQ)

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.

K972397EZ SPRAYIntertex Research, Inc.K964956E-Z SPACER MASK (SMALL)Airpharma, LLCK961894MDI TUTORMdi Tutor, Inc.K961455MEDSHIELD/AEROCHAMBERDiemolding Corp.K960593SMARTMIST ASTHMA MANAGMENT SYSTEM, SMARTMIST, MODEL NUMBER SM-100/SMARTMIST SPIROMETRY AIRWAY, MODEL NUMBER SA-100Aradigm Corp.K922033SALINE SOLUTION- STERILETrinity Laboratories, 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.

↑