ClearanceBrief
510(k) K904172 ยท GDF Guide, Needle, Surgical

ACCUPLACE (TM)

ApplicantDlp, Inc., Grand Rapids MI, US
DecisionSubstantially Equivalent, Nov 21, 1990
ReceivedSep 11, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904172

DateFirm and productCodeLinked 510(k)
Mar 3, 2016Stryker Instruments Div. of Stryker Corporation
(Stryker) AccuPlace Straight Level Needle Guide; Assists the user with inserting a needle at a predetermined angle for computer tomography.
Terminated
GDFNone listed
Mar 3, 2016Stryker Instruments Div. of Stryker Corporation
(Stryker) AccuPlace Round Level Needle Guide; Assists the user with inserting a needle at a predetermined angle for computer tomography.
Terminated
GDFNone listed
Mar 3, 2016Stryker Instruments Div. of Stryker Corporation
50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide; Assists the user with inserting a needle at a predetermined angle for computer tomography.
Terminated
GDFNone listed
Mar 3, 2016Stryker Instruments Div. of Stryker Corporation
50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide; Assists the user with inserting a needle at a predetermined angle for computer tomography.
Terminated
GDFNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.