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510(k) Data Aggregation

    K Number
    K980001
    Device Name
    JENASCAN
    Date Cleared
    1998-03-19

    (76 days)

    Product Code
    Regulation Number
    878.4810
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    JENASCAN

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The JENASCAN is intended for use as an accessory to surgical lasers, e.g., lasers used in dermatology and plastic surgery, for the ablation and vaporization of soft tissue under conditions of use as described in the manuals accompanying the lasers.

    Please refer to the application, operator's, or user's manual(s) accompanying the laser for professional use instructions and detailed use information concerning the laser.

    Device Description

    The Jenoptik JENASCAN is a microprocessor-controlled accessory for lasers used in dermatology and plastic surgery. The JENASCAN guides the laser energy over the skin during removal of soft tissue under the conditions of labeling as described in the laser operator's manual.

    AI/ML Overview

    The provided document is a 510(k) summary for the JENOPTIK JENASCAN, a laser accessory. It explicitly states that no performance data were required or provided because the device is considered substantially equivalent to already legally marketed predicate devices. Therefore, the requested information regarding acceptance criteria, study details, and performance metrics cannot be extracted from this document.

    The relevant section from the document states:

    "Performance Data: None. The specifications and intended uses of the Jenoptik JENASCAN are the same or very similar to those of the claimed predicate devices. There are no significant differences between the devices under conditions of intended use. Because of this, performance data were not required."

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