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A SLEEP APNEA THERAPY DEVICE for anytime and anywhere3 Bongo Rx is an FDA cleared EPP device for treating mild to moderate obstructive sleep apnea (OSA)3 No machine, hose, electricity or batteries
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What is 18001a bongo rx brochure?
18001a bongo rx brochure is a document that provides information about the Bongo RX model for the year 18001a.
Who is required to file 18001a bongo rx brochure?
All manufacturers and distributors of the Bongo RX model for the year 18001a are required to file the brochure.
How to fill out 18001a bongo rx brochure?
The brochure should be filled out with accurate information about the Bongo RX model, including specifications, features, and any relevant safety information.
What is the purpose of 18001a bongo rx brochure?
The purpose of the brochure is to provide consumers and regulators with detailed information about the Bongo RX model for the year 18001a.
What information must be reported on 18001a bongo rx brochure?
The brochure must include details such as engine specifications, safety features, fuel efficiency, and any special features of the Bongo RX model.
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