BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

    PHILIPS SOLARIUM HP 3134

    K Number: K852348 · Decision Jun 27, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    25
    Registration Numbers
    25
    Same Product Code
    271
    Applicant Total
    11
    Review Days
    27

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    Basic Information

    Device Name
    PHILIPS SOLARIUM HP 3134
    K Number
    K852348
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4630
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Philips Int'L B.V.
    Date Received
    May 31, 1985
    Decision Date
    June 27, 1985
    Product Code
    FTC
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FTC Light, Ultraviolet, Dermatological

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    Other Clearances by Philips Int'L B.V.

    K Number Device Name
    K920134 PHILIPS 41 SERIES RAINBOW
    K920142 PHILIPS M60 SERIES
    K851534 PHILIPS UV-A SOLARIUM TYPE HP 3150
    K851536 PHILIPS UV-A SOLARIUM TYPE HP 3141
    K851535 PHILIPS UV-A SOLARIUM TYPE HP 3140
    K851533 PHILIPS UV-A SDARIUM TYPE HP 3148(CFR 21 SUNLAMP
    K850206 PHILIPS UV-A SOLARIUM TYPE HP 3126-SUNLAMP
    K850205 PHILIPS UV-A SOLARIUM TYPE HP 3127-SUNLAMP
    K850203 PHILIPS UV-A SOLARIUM TYPE HP 3016-SUNLAMP
    K850204 PHILIPS UV-A SOLARIUM TYPE HP 3130-SUNLAMP
    Search all 11 clearances from Philips Int'L B.V. →