FDA 510(k) Applications Submitted by WELCH ALLYN PROTOCOL, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K033378 |
10/22/2003 |
VITAL SIGNS MONITOR, PROPAQ LT |
WELCH ALLYN PROTOCOL, INC. |
| K021681 |
05/22/2002 |
MICROPAQ, MODELS 402, 404 |
WELCH ALLYN PROTOCOL, INC. |
| K022453 |
07/26/2002 |
MODIFICATION TO ACUITY CENTRAL MONITORING SYSTEM |
WELCH ALLYN PROTOCOL, INC. |
| K012451 |
08/01/2001 |
PROPAQ ENCORE MODELS 202, 204, 206; PROPAQ CS MODELS 242, 244, 246 |
WELCH ALLYN PROTOCOL, INC. |
| K031740 |
06/04/2003 |
VSM - VITAL SIGNS MONITOR, MODEL 53000 SERIES |
WELCH ALLYN PROTOCOL, INC. |
| K070204 |
01/22/2007 |
LINK TO ACUITY CLINICIAN NOTIFIER |
WELCH ALLYN PROTOCOL, INC. |
| K063419 |
11/13/2006 |
MODIFICATION TO VSM- VITAL SIGNS MONITOR, (VSM 300 ) |
WELCH ALLYN PROTOCOL, INC. |
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