The following data is part of a premarket notification filed by Welch Allyn, Inc. with the FDA for Vital Signs Monitor, Connex Vital Signs Monitor.
Device ID | K132808 |
510k Number | K132808 |
Device Name: | VITAL SIGNS MONITOR, CONNEX VITAL SIGNS MONITOR |
Classification | Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms) |
Applicant | WELCH ALLYN, INC. 4341 STATE ST. RD. P.O. BOX 220 Skaneateles Falls, NY 13153 -0220 |
Contact | Kevin Crossen |
Correspondent | Kevin Crossen WELCH ALLYN, INC. 4341 STATE ST. RD. P.O. BOX 220 Skaneateles Falls, NY 13153 -0220 |
Product Code | MWI |
CFR Regulation Number | 870.2300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-09-11 |
Decision Date | 2013-11-20 |
Summary: | summary |