(243 days)
The Crescent Sound Generator is an electronic, air-conduction broadband noise generator intended to generate noise of sufficient intensity and bandwidth to be used for tinnitus masking therapy. The Crescent Sound Generator is intended to be used by those individuals who experience tinnitus, and do not need or desire amplification. The intended use of this device includes it's fitting by a qualified audiologist or other hearing healthcare professional familiar with the diagnosis and treatment of tinnitus.
The Crescent Sound Generator is an electronic, air-conduction broadband noise generator intended to generate noise of sufficient intensity and bandwidth to be used for tinnitus masking therapy.
This document is a 510(k) clearance letter from the FDA for a device called "Crescent Sound Generator." It does not contain information about acceptance criteria or a study proving the device meets said criteria. Therefore, I cannot provide the requested information based on the given text.
The document states that the FDA has determined the device is substantially equivalent to legally marketed predicate devices. This determination is typically based on comparing the new device to existing ones, rather than requiring the new device to meet specific performance acceptance criteria through a dedicated study as one might see for novel technologies.
The 510(k) process primarily focuses on demonstrating substantial equivalence in terms of intended use, technological characteristics, and safety and effectiveness compared to a predicate device. It does not typically involve the detailed performance studies, acceptance criteria, and ground truth establishment associated with AI/ML devices or more innovative medical devices that might require a PMA or de novo clearance.
§ 874.3400 Tinnitus masker.
(a)
Identification. A tinnitus masker is an electronic device intended to generate noise of sufficient intensity and bandwidth to mask ringing in the ears or internal head noises. Because the device is able to mask internal noises, it is also used as an aid in hearing external noises and speech.(b)
Classification. Class II. The special control for this device is patient labeling regarding:(1) Hearing health care professional diagnosis, fitting of the device, and followup care,
(2) Risks,
(3) Benefits,
(4) Warnings for safe use, and
(5) Specifications.