FDA 510(k) Applications Submitted by JOHN E SAWYER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K070060 |
01/05/2007 |
WELCH ALLYN FLEXIPORT DISPOSABLE BLOOD PRESSURE CUFF (ONE-PIECE); REUSABLE BLOOD PRESSURE CUFF (ONE-PIECE) |
WELCH ALLYN, INC. |
| K082478 |
08/28/2008 |
WELCH ALLYN CARDIOPERFECT WORKSTATION SOFTWARE (CPWS) V 1.62 |
WELCH ALLYN, INC. |
| K072449 |
08/31/2007 |
CP100 & 200 12-LEAD RESTING ELECTROCARDIOGRAPHS |
WELCH ALLYN, INC. |
| K031225 |
04/17/2003 |
TIMESH ALSO KNOWN AS TIMESH-TC, MODELS 6000001 & 6000004 |
GFE MEDIZINTECHNIK GMBH |
| K071218 |
05/02/2007 |
PROXENON 350, MODEL 902XX |
WELCH ALLYN, INC. |
| K052160 |
08/09/2005 |
ACUITY CENTRAL STATION, MODEL 020XXXXX (NOTE: XXXXX = VARIOUS CONFIG.) |
WELCH ALLYN, INC. |
| K053027 |
10/27/2005 |
VSM VITAL SIGNS MONITOR, MODEL 53000 (VSM 300) |
WELCH ALLYN, INC. |
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