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)

RC CORNET, MODEL #44F50

K-Number: K983308 · 1999-06-04

ApplicantPari Holding Co.
Decision Date1999-06-04
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RC CORNET, MODEL #44F50 is the device name listed in this FDA 510(k) record. The listed applicant is Pari Holding Co.. It received FDA 510(k) clearance on 1999-06-04 under 510(k) number K983308. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RC CORNET, MODEL #44F50?

RC CORNET, MODEL #44F50 is a medical device that received FDA 510(k) clearance on 1999-06-04. The listed applicant is Pari Holding Co.. The 510(k) number is K983308.

When did RC CORNET, MODEL #44F50 receive FDA 510(k) clearance?

RC CORNET, MODEL #44F50 received FDA 510(k) clearance on 1999-06-04, under 510(k) number K983308.

Who is the listed applicant for RC CORNET, MODEL #44F50?

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

What is the FDA product code for RC CORNET, MODEL #44F50?

The FDA product code for RC CORNET, MODEL #44F50 is BWF.

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 Pari Holding Co. 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.

K002862PRONEB ULTRA MODEL NUMBER 85B0100K972042PARI PEP THERAPY SYSTEMK963924LC STAR REUSABLE NEBULIZER 22F50 AND LC STAR DISPOSABLE NEBULIZER 22F70K962072PRONEB TURBO COMPRESSOR MODEL 38V0200K960675WALKHALER PORTABLE COMPRESSOR MODEL 45F70K935540PARI-MASTER MODIFICATION

View all 8 devices →

Related Devices (Code: BWF)

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.

K241152InSeeTidal Medical Technologies, LLCK233855AllPEPEnchant Tek Co. , Ltd.K221058LungTrainer (MD2 & MD3)Lung Trainers, LLCK222018Breathe+Peep Medical, LLC Dba Go2 DevicesK220565Hudson RCI Triflo II Incentive Deep Breathing ExerciserMedline Industries, Inc.K203378PulsehalerRespinova, Ltd.

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.

↑