FDA 510(k) Applications Submitted by WILLIAM E ANSPACH III
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K011176 |
04/17/2001 |
REUSABLE GLASS SYRINGES |
LOCKETT MEDICAL CORP. |
K970530 |
02/12/1997 |
ANSPACH LUBRICATING SYSTEM II |
THE ANSPACH EFFORT, INC. |
K002903 |
09/18/2000 |
ANSPACH ANGLED MICRONOSE ATTACHMENT |
THE ANSPACH EFFORT, INC. |
K974025 |
10/23/1997 |
ANSPACH SHIELDED ATTACHMENT |
THE ANSPACH EFFORT, INC. |
K981688 |
05/11/1998 |
ANSPACH SUTURE ANCHOR |
THE ANSPACH EFFORT, INC. |
K963686 |
09/12/1996 |
ANSPACH SUTURE ANCHOR (MODIFIED) |
THE ANSPACH EFFORT, INC. |
K965080 |
12/19/1996 |
ANSPACH MICROMAX SYSTEM |
THE ANSPACH EFFORT, INC. |
K111133 |
04/22/2011 |
NON-STERILE, POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEIN CLAIM (50 MG OR LESS) |
SSC SURAT THANI |
K111134 |
04/22/2011 |
NON-STERILE, POWDER-FREE NITRILE EXAMINATION GLOVE, BLUE, TESTED FOR USE WITH CHEMOTHERAPY DRUGS |
SIEM AEMPEMED CORP., LTD |
K955528 |
12/04/1995 |
CLP BONNET |
CLP PRODUCTS |
K970927 |
03/13/1997 |
BRUNO ELECTRA-RIDE III STAIRWAY ELEVATOR SYSTEM |
BRUNO INDEPENDENT LIVING AIDS, INC. |
K991954 |
06/10/1999 |
THE BRUNO POWERBASE, MODEL PSB-2200 |
BRUNO INDEPENDENT LIVING AIDS, INC. |
|
|