FDA 510(k)

Prosomnus [CA] Schlaf- und Schnarchgerät und Prosomnus [CA] Schlaf- und Schnarchgerät mit Mikro-Rekorder

K-Nummer: K172859 · 2017-11-22

AntragstellerProsomnous Sleep Technologies

Entscheidungsdatum2017-11-22

ProduktcodePLC

BeratungsausschussDE

EntscheidungSubstantially Equivalent

Produktübersicht

Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder is the device name listed in this FDA 510(k) record. The listed applicant is Prosomnous Sleep Technologies. It received FDA 510(k) clearance on 2017-11-22 under 510(k) number K172859. The device is classified under product code PLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder?

Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder is a medical device that received FDA 510(k) clearance on 2017-11-22. The listed applicant is Prosomnous Sleep Technologies. The 510(k) number is K172859.

When did Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder receive FDA 510(k) clearance?

Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder received FDA 510(k) clearance on 2017-11-22, under 510(k) number K172859.

Who is the listed applicant for Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder?

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

What is the FDA product code for Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder?

The FDA product code for Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder is PLC.

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Verwandte Geräte (Code: PLC)

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