FDA 510(k) Applications for Medical Device Product Code "LKG"
(Port & Catheter, Implanted, Subcutaneous, Intraventricular)

FDA 510(k) Number Applicant Device Name Decision Date
K823790 AMERICAN HEYER SCHULTE VENTRICULAR ACCESS SYSTEM 04/28/1983
K950315 CORDIS CORP. CORDIS CSF RESERVOIR 05/09/1995
K833672 HOLTER-HAUSNER INTL. HH SUBCUTANEOUS ACCESS PORT 03/06/1984
K881493 PHARMACIA DELTEC, INC. PORT-A-CATH IMPLANTABLE ACCESS SYSTEM - KIT CONF. 05/20/1988
K881690 PHARMACIA DELTEC, INC. PORT-A-CATH PORTAL INTRODUCER FORCEPS 05/20/1988
K874498 PUDENZ-SCHULTE MEDICAL RESEARCH CORP. CSF-VENTRICULOSTOMY RESERVOIR 02/11/1988
K833822 PUDENZ-SCHULTE MEDICAL RESEARCH CORP. P-S MEDICAL CSF ACCESS DEV 15MM/25MM 05/25/1984
K874468 PUDENZ-SCHULTE MEDICAL RESEARCH CORP. P-S MEDICAL VENTRICULAR ACCESS PORT 02/11/1988


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