FDA 510(k) Applications Submitted by DAVID DING
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K040315 |
02/09/2004 |
MYOHEALTH CLENCHING INHIBITOR |
MCI-MYOHEALTH SYSTEMS |
K003517 |
11/14/2000 |
OTRES TOOTHBRUSH SANITIZER MODEL TB100W |
OTRES, LLC. |
K072223 |
08/10/2007 |
VINYL EXAMINATION GLOVE, POWDERED |
PINNACLE CO., LTD. |
K072227 |
08/10/2007 |
VINYL EXAMINATION GLOVE POWDER FREE |
PINNACLE CO., LTD. |
K072228 |
08/10/2007 |
SYNTHETIC VINYL EXAMINATION GLOVE POWDER FREE (YELLOW/WHITE) |
PINNACLE CO., LTD. |
K970521 |
02/11/1997 |
TRX POWER TILT AND RECLINE SYSTEM |
MOTION CONCEPTS |
K981837 |
05/26/1998 |
TRX-CG CENTER-OF-GRAVITY SHIFTING POWER TILT AND RECLINE SYSTEMS |
MOTION CONCEPTS |
K960371 |
01/26/1996 |
INTERPORE THREADED IMPLANT |
INTERPORE INTL. |
K980817 |
03/03/1998 |
PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30L |
INTERPORE INTL. |
K972842 |
08/01/1997 |
INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE |
INTERPORE INTL. |
K955492 |
12/01/1995 |
INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLT |
INTERPORE INTL. |
|
|