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FDA 510(k)

LUNG TECHNOLOGIES 5000 THERAPEUTIC INCENTIVE SPIROMETER

K-Number: K944344 · 1995-02-03

ApplicantLung Technologies, Inc.
Decision Date1995-02-03
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LUNG TECHNOLOGIES 5000 THERAPEUTIC INCENTIVE SPIROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Lung Technologies, Inc.. It received FDA 510(k) clearance on 1995-02-03 under 510(k) number K944344. 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 LUNG TECHNOLOGIES 5000 THERAPEUTIC INCENTIVE SPIROMETER?

LUNG TECHNOLOGIES 5000 THERAPEUTIC INCENTIVE SPIROMETER is a medical device that received FDA 510(k) clearance on 1995-02-03. The listed applicant is Lung Technologies, Inc.. The 510(k) number is K944344.

When did LUNG TECHNOLOGIES 5000 THERAPEUTIC INCENTIVE SPIROMETER receive FDA 510(k) clearance?

LUNG TECHNOLOGIES 5000 THERAPEUTIC INCENTIVE SPIROMETER received FDA 510(k) clearance on 1995-02-03, under 510(k) number K944344.

Who is the listed applicant for LUNG TECHNOLOGIES 5000 THERAPEUTIC INCENTIVE SPIROMETER?

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

What is the FDA product code for LUNG TECHNOLOGIES 5000 THERAPEUTIC INCENTIVE SPIROMETER?

The FDA product code for LUNG TECHNOLOGIES 5000 THERAPEUTIC INCENTIVE SPIROMETER is BWF.

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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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