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510(k) Data Aggregation

    K Number
    K000905
    Device Name
    URETHROTOME 8667.XXX AND 8670.XXX
    Manufacturer
    RICHARD WOLF MEDICAL INSTRUMENTS CORP.
    Date Cleared
    2000-05-12

    (52 days)

    Product Code
    EZO
    Regulation Number
    876.4770
    Why did this record match?
    Product Code :

    EZO

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
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    K Number
    K950719
    Device Name
    OES UROLOGY
    Manufacturer
    OLYMPUS AMERICA, INC.
    Date Cleared
    1996-12-11

    (664 days)

    Product Code
    EZO
    Regulation Number
    876.4770
    Why did this record match?
    Product Code :

    EZO

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Olympus 00216 Otis Urethrotome and 02160 Replacement Blade are intended to be used for endoscopic and treatment within the urethra in adults. When compared with the intended use of predicate devices, the intended use of the subject devices has not been changed. Olympus 02161 Otis Urethrotome and 02162 Replacement Blade are intended to be used for endoscopic treatment within the urethra in children. When compared with the predicate devices, the Olympus subject devices are intended for pediatric use, while the Olympus predicate devices were cleared for Infant Use in 510(k) # K904940.
    Device Description
    Olympus America Inc. has been marketing rigid endoscopes, hand instruments, associated accessories, and ancillary equipment for Urological Endoscopy since 1979. The Olympus Urethrotomy System includes the following products. - 1. Otis Urethrotome for Adult Use - 00216 Otis Urethrotome, 16 cm - - Replacement Blade for 00216 Urethrotome -02160 - 2. Otis Urethrotome for Pediatric Use - 02161 Otis Urethrotome, 10.5 cm - - 02162 Replacement Blade for O2162 Urethrotome ・ When these subject devices are compared with the predicate devices, which were cleared in 510(k)s # K790071 and K904940, no significant changes or modifications in intended use, design, material, function, method of operation, or reprocessing that could affect the safety and efficacy of the devices have occurred.
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