BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    CIRCUIT TREE PHACOEMULSIFIER

    K Number: K954242 · Decision Dec 1, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    73
    Registration Numbers
    73
    Same Product Code
    315
    Applicant Total
    3
    Review Days
    81

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    CIRCUIT TREE PHACOEMULSIFIER
    K Number
    K954242
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.4670
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Circuit Tree
    Date Received
    September 11, 1995
    Decision Date
    December 1, 1995
    Product Code
    HQC
    Advisory Committee
    Ophthalmic
    Review Advisory Committee
    OP
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HQC Unit, Phacofragmentation

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (HQC), ordered by most recent decision date.

    Stellaris Elite™ vision enhancement system; Posterior and Combined Procedure Pack(s): 23 ga. Posterior Elite™ Pack (SE5423); 23 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423B); 25 ga. Posterior Elite™ Pack (SE5425); 25 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5425B); 27 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5427B); 23 ga. Bi-Blade™+ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423BB+); 25 ga. Bi-Blade™+

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Stellaris Elite™ vision enhancement system (BL11145, BL14455, BL15455, SE14565, SE15565, SE14565E, SE15565E)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    System Sophi

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MICOR 700 with Auto I/A

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Stellaris Elite vision enhancement system (BL11145, BL14455, BL15455)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic
    View all

    Other Clearances by Circuit Tree

    K Number Device Name
    K981989 THE WAVE DIGITAL PHACO SYSTEM
    K954237 CIRCUIT TREE PHACO HANDPIECE