FDA 510(k) Applications Submitted by CHARLES H KYPER
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K020584 |
02/21/2002 |
N2000 BASE STATION; N2001 NURSE STATION |
NEPTEC DESIGN GROUP, LTD. |
K010813 |
03/19/2001 |
SIMPLICT |
NEORAD AS |
K000932 |
03/23/2000 |
ARACHNOPHLEBECTOMY NEEDLE |
ADVANCED MEDICAL PRODUCTS, INC. |
K010933 |
03/28/2001 |
SEAL-ON TOPICAL HEMPSTATIC POWDER SPRAY |
ALLTRACEL PHARMA LTD. |
K991367 |
04/20/1999 |
MEDITRON STETHOSCOPE SYSTEM |
MEDITRON AS |
K012429 |
07/31/2001 |
SURESET INFUSION SET, MODEL 8023 |
APPLIED DIABETES RESEARCH, INCORPORATED |
K012801 |
08/21/2001 |
N2000 BASE STATION, N2001 NURSE STATION |
NEPTEC DESIGN GROUP, LTD. |
K062444 |
08/21/2006 |
HI-SLIP AND HI-SLIP PLUS SINGLE USE HYDROPHILIC URINARY CATHETERS AND KIT |
OASIS MEDIKAL URUNLER KIMYA SANAYI VE TIC A.S. |
K003130 |
10/06/2000 |
REGUTHERM 952 THERMOGRAPHIC SYSTEM |
SIE-MED, INC. |
K023367 |
10/08/2002 |
DETECTAR, MODEL N123-MI |
NEKS TECHNOLOGIES |
K964083 |
10/11/1996 |
ULTRATHERM (908) |
SIE-MED, INC. |
K013725 |
11/09/2001 |
MEDITRON II THESTERTHOSCOPE SYSTEM |
MEDITRON AS |
K043156 |
11/15/2004 |
D-CARIE, MODEL N121-M1 |
NEKS TECHNOLOGIES, INC. |
|
|