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)

INSPIRATORY/EXPIRATORY MUSCLE EXERCIS

K-Number: K840418 · 1984-02-17

ApplicantInspiron Corp.
Decision Date1984-02-17
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INSPIRATORY/EXPIRATORY MUSCLE EXERCIS is the device name listed in this FDA 510(k) record. The listed applicant is Inspiron Corp.. It received FDA 510(k) clearance on 1984-02-17 under 510(k) number K840418. 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 INSPIRATORY/EXPIRATORY MUSCLE EXERCIS?

INSPIRATORY/EXPIRATORY MUSCLE EXERCIS is a medical device that received FDA 510(k) clearance on 1984-02-17. The listed applicant is Inspiron Corp.. The 510(k) number is K840418.

When did INSPIRATORY/EXPIRATORY MUSCLE EXERCIS receive FDA 510(k) clearance?

INSPIRATORY/EXPIRATORY MUSCLE EXERCIS received FDA 510(k) clearance on 1984-02-17, under 510(k) number K840418.

Who is the listed applicant for INSPIRATORY/EXPIRATORY MUSCLE EXERCIS?

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

What is the FDA product code for INSPIRATORY/EXPIRATORY MUSCLE EXERCIS?

The FDA product code for INSPIRATORY/EXPIRATORY MUSCLE EXERCIS 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 Inspiron 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.

K860838INSPIRON DOUBLE SWIVEL TRACH ADAPTERK850346OXYGEN CONCENTRATORK843932VAPOR-PHASE HUMIDIFIER SYS-ADVANCEDK840935MANUAL RESUSCITATION SYSTEMK841158NEBULO 28 NEBULIZER KITK834290INSPIRON LIQUID OXYGEN SYSTEM

View all 20 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.

↑