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FDA 510(k)

INSPIROMETER RESPIRATORY EXERCISER

K-Number: K770141 · 1977-02-01

ApplicantMedi, Inc.
Decision Date1977-02-01
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INSPIROMETER RESPIRATORY EXERCISER is the device name listed in this FDA 510(k) record. The listed applicant is Medi, Inc.. It received FDA 510(k) clearance on 1977-02-01 under 510(k) number K770141. 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 INSPIROMETER RESPIRATORY EXERCISER?

INSPIROMETER RESPIRATORY EXERCISER is a medical device that received FDA 510(k) clearance on 1977-02-01. The listed applicant is Medi, Inc.. The 510(k) number is K770141.

When did INSPIROMETER RESPIRATORY EXERCISER receive FDA 510(k) clearance?

INSPIROMETER RESPIRATORY EXERCISER received FDA 510(k) clearance on 1977-02-01, under 510(k) number K770141.

Who is the listed applicant for INSPIROMETER RESPIRATORY EXERCISER?

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

What is the FDA product code for INSPIROMETER RESPIRATORY EXERCISER?

The FDA product code for INSPIROMETER RESPIRATORY EXERCISER is BWF.

Related Clinical Trials

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Other records listing Medi, Inc. 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.

K771121EMPTY ADMIXTURE CONTAINERS

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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