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FDA 510(k)

MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER

K-Number: K871742 · 1987-06-15

ApplicantHealth Products, Inc.
Decision Date1987-06-15
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER is the device name listed in this FDA 510(k) record. The listed applicant is Health Products, Inc.. It received FDA 510(k) clearance on 1987-06-15 under 510(k) number K871742. 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 MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER?

MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER is a medical device that received FDA 510(k) clearance on 1987-06-15. The listed applicant is Health Products, Inc.. The 510(k) number is K871742.

When did MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER receive FDA 510(k) clearance?

MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER received FDA 510(k) clearance on 1987-06-15, under 510(k) number K871742.

Who is the listed applicant for MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER?

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

What is the FDA product code for MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER?

The FDA product code for MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER is BWF.

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Other records listing Health Products, Inc. as applicant

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K912866PEAK EXPIRATORY FLOW METERK912943THRESHOLD 2X INSPIRATORY MUSCLE TRAINERK911807METERED DOSE INHALER (MDI) SPACERK902292MODIFIED ASSESS(R) PEAK FLOW METERK896953MODIFIED ASSESS(R) PEAK FLOW METERK894353ORTHODERM CONVERTIBLE

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Related Devices (Code: BWF)

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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.

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