FDA 510(k) Applications Submitted by EDWARD M BASILE
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K060305 |
02/06/2006 |
HAIRMAX LASERCOMB |
LEXINGTON INTERNATIONAL, LLC |
K021097 |
04/04/2002 |
QUEST EXERCISE STRESS SYSTEM (QUEST), VERSION 3.52 |
SPACELABS MEDICAL, INC. |
K991458 |
04/26/1999 |
MECA WRIST BLOOD PRESSURE METER, MODEL EW243 AND MODEL EW254 |
MATSUSHITA ELECTRIC CORP. OF AMERICA |
K981542 |
04/29/1998 |
PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284 |
PANASONIC CORPORATION (PANASONIC) |
K051284 |
05/13/2005 |
MD TURBO |
RESPIRICS, INC. |
K962261 |
06/12/1996 |
IMPLANTECH WM NASAL-LABIAL IMPLANT |
IMPLANTECH ASSOCIATES, INC. |
K962824 |
07/19/1996 |
IMPLANTECH JEJ PERI-PYRIFORM IMPLANT |
IMPLANTECH ASSOCIATES, INC. |
K013046 |
09/10/2001 |
COSMOS SYSTEM |
SPACELABS MEDICAL, INC. |
K973502 |
09/16/1997 |
IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT |
IMPLANTECH ASSOCIATES, INC. |
K981431 |
04/20/1998 |
PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW280 |
PANASONIC CORPORATION (PANASONIC) |
K964846 |
12/03/1996 |
IMPLATECH RP MEDICAL GRADE SILICONE GEL SHEETING |
IMPLANTECH ASSOCIATES, INC. |
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