FDA 510(k)

Solar Storm, Solar Wave, Sunco, and ESB (Avalon, Galaxy, Grande, Oasis, Elite and Leisure Select)

K-Nummer: K180576 · 2018-04-19

Entscheidungsdatum2018-04-19

ProduktcodeLEJ

BeratungsausschussSU

EntscheidungSubstantially Equivalent

Produktübersicht

Solar Storm, Solar Wave, Sunco, and ESB (Avalon, Galaxy, Grande, Oasis, Elite and Leisure Select) is the device name listed in this FDA 510(k) record. The listed applicant is Lpi, Inc.. It received FDA 510(k) clearance on 2018-04-19 under 510(k) number K180576. The device is classified under product code LEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the Solar Storm, Solar Wave, Sunco, and ESB (Avalon, Galaxy, Grande, Oasis, Elite and Leisure Select)?

Solar Storm, Solar Wave, Sunco, and ESB (Avalon, Galaxy, Grande, Oasis, Elite and Leisure Select) is a medical device that received FDA 510(k) clearance on 2018-04-19. The listed applicant is Lpi, Inc.. The 510(k) number is K180576.

When did Solar Storm, Solar Wave, Sunco, and ESB (Avalon, Galaxy, Grande, Oasis, Elite and Leisure Select) receive FDA 510(k) clearance?

Solar Storm, Solar Wave, Sunco, and ESB (Avalon, Galaxy, Grande, Oasis, Elite and Leisure Select) received FDA 510(k) clearance on 2018-04-19, under 510(k) number K180576.

Who is the listed applicant for Solar Storm, Solar Wave, Sunco, and ESB (Avalon, Galaxy, Grande, Oasis, Elite and Leisure Select)?

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

What is the FDA product code for Solar Storm, Solar Wave, Sunco, and ESB (Avalon, Galaxy, Grande, Oasis, Elite and Leisure Select)?

The FDA product code for Solar Storm, Solar Wave, Sunco, and ESB (Avalon, Galaxy, Grande, Oasis, Elite and Leisure Select) is LEJ.

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Verwandte Geräte (Code: LEJ)

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Offizielle Quelle

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