FDA 510(k) Applications Submitted by AMY J LAFORTE, PH.D.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K963577 |
09/06/1996 |
RADIONICS SLUIJTER-MEHTA CANNULA |
RADIONICS, INC. |
K962155 |
06/04/1996 |
GILL-THOMAS-COSMAN(GTC) DENTAL TRAY |
RADIONICS SOFTWARE APPLICATIONS, INC. |
K960071 |
01/05/1996 |
IMAGEFUSION |
RADIONICS SOFTWARE APPLICATIONS, INC. |
K961942 |
05/20/1996 |
EPIDURAL PEG ELECTRODE (EP), SPHENOIDAL ELECTRODE (EDS) AND FORAMEN, OVALE DEPTH ELECTRODE (ED-FO) FOR EPILEPSY MONITORI |
RADIONICS, INC. |
K965182 |
12/24/1996 |
RFG-3CF |
RADIONICS, INC. |
K961858 |
05/14/1996 |
COSGROVE DEPTH ELECTRODE KIT(CDEK) |
RADIONICS, INC. |
K963579 |
09/06/1996 |
PACE-1A CARDIAC STIMULATOR |
RADIONICS, INC. |
K961844 |
05/13/1996 |
OPERATING ARM SYSTEM (OAS) [WITH CT AND MR IMAGES] |
RADIONICS SOFTWARE APPLICATIONS, INC. |
K964801 |
11/29/1996 |
OPTICAL TRACKING SYSTEM (OTS) |
RADIONICS SOFTWARE APPLICATIONS, INC. |
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