FDA 510(k) Applications Submitted by WILLIAM LOCKETT 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. |
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