FDA 510(k) Applications Submitted by NANCY J GERTLAR
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K010623 |
03/02/2001 |
RECONSTITUTION KIT & VIAL CONNECTOR |
BIOJECT, INC. |
| K030763 |
03/11/2003 |
DIAGNOSTIC ULTRASOUND BLADDERMASS BVM 6500 ULTRASOUND SYSTEM |
DIAGNOSTIC ULTRASOUND CORP. |
| K981655 |
05/11/1998 |
SPACELABS MEDICAL DISPOSABLE SP02 SENSOR |
SPACELABS MEDICAL, INC. |
| K992749 |
08/16/1999 |
ULTRAVIEW WAVEFORM PAGER SYSTEM, MODEL 91841 |
SPACELABS MEDICAL, INC. |
| K082366 |
08/18/2008 |
LIFEBED PATIENT VIGILANCE SYSTEM |
HOANA MEDICAL, INC. |
| K133116 |
09/30/2013 |
VIDEO EXTENDED LENGTH TRAY (PLASTIC - RADEL), VIDEO TRAY SINGLE LEVEL (PLASTIC - RADEL), VIDEO ARTHROSCOPE TRAY (PLASTIC |
CONMED CORPORATION |
| K083534 |
11/28/2008 |
LIFEBED NETWORK PATIENT VIGILANCE SYSTEM |
HOANA MEDICAL, INC. |
| K994384 |
12/28/1999 |
CLICKER |
BIOJECT, INC. |
| K983996 |
11/10/1998 |
SPACELABS MEDICAL ULTRAVIEW DIGITAL TELEMTRY SYSTEM |
SPACELABS MEDICAL, INC. |
| K003908 |
12/19/2000 |
SEROJET |
BIOJECT, INC. |
| K172384 |
08/08/2017 |
Quickie(r) Q700-UP M |
Sunrise Medical (US) LLC |
|
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