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FDA 510(k)

BAG, POST OPERATIVE LUNG EXERCIZING BLOW

K-Number: K760167 · 1976-08-06

ApplicantDytek Corp.
Decision Date1976-08-06
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BAG, POST OPERATIVE LUNG EXERCIZING BLOW is the device name listed in this FDA 510(k) record. The listed applicant is Dytek Corp.. It received FDA 510(k) clearance on 1976-08-06 under 510(k) number K760167. 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 BAG, POST OPERATIVE LUNG EXERCIZING BLOW?

BAG, POST OPERATIVE LUNG EXERCIZING BLOW is a medical device that received FDA 510(k) clearance on 1976-08-06. The listed applicant is Dytek Corp.. The 510(k) number is K760167.

When did BAG, POST OPERATIVE LUNG EXERCIZING BLOW receive FDA 510(k) clearance?

BAG, POST OPERATIVE LUNG EXERCIZING BLOW received FDA 510(k) clearance on 1976-08-06, under 510(k) number K760167.

Who is the listed applicant for BAG, POST OPERATIVE LUNG EXERCIZING BLOW?

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

What is the FDA product code for BAG, POST OPERATIVE LUNG EXERCIZING BLOW?

The FDA product code for BAG, POST OPERATIVE LUNG EXERCIZING BLOW 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.

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Other records listing Dytek 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.

K781245LUNG EXER. BAG, POST-OP, MODIFIEDK760168PENCIL, ELECTROSURGICAL

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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