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)

ROSENTHAL-FRENCH NEBULIZATION DOSIMETER

K-Number: K860800 · 1986-03-27

ApplicantLaboratory For Applied Immunology, Inc.
Decision Date1986-03-27
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ROSENTHAL-FRENCH NEBULIZATION DOSIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Laboratory For Applied Immunology, Inc.. It received FDA 510(k) clearance on 1986-03-27 under 510(k) number K860800. 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 ROSENTHAL-FRENCH NEBULIZATION DOSIMETER?

ROSENTHAL-FRENCH NEBULIZATION DOSIMETER is a medical device that received FDA 510(k) clearance on 1986-03-27. The listed applicant is Laboratory For Applied Immunology, Inc.. The 510(k) number is K860800.

When did ROSENTHAL-FRENCH NEBULIZATION DOSIMETER receive FDA 510(k) clearance?

ROSENTHAL-FRENCH NEBULIZATION DOSIMETER received FDA 510(k) clearance on 1986-03-27, under 510(k) number K860800.

Who is the listed applicant for ROSENTHAL-FRENCH NEBULIZATION DOSIMETER?

The FDA 510(k) record lists Laboratory For Applied Immunology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROSENTHAL-FRENCH NEBULIZATION DOSIMETER?

The FDA product code for ROSENTHAL-FRENCH NEBULIZATION DOSIMETER 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

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.

↑