Atlas FDA

WELCH ALLYN, INC/MORTARA

10 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch WELCH ALLYN, INC/MORTARA

RecordFirmDate
Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI recall (Z-1810-2020)WELCH ALLYN, INC/MORTARA2020-04-29
ELI PC. The ELI PC Service automatically converts resting ECG recordings collected with WA recall (Z-1811-2020)WELCH ALLYN, INC/MORTARA2020-04-29
H12+ and patient cable for the H12+ Holter Recorders with the following device name: PAT C recall (Z-1812-2020)WELCH ALLYN, INC/MORTARA2020-04-29
T12. Incorporates wireless electrocardiographic technology to achieve the real-time acquis recall (Z-1813-2020)WELCH ALLYN, INC/MORTARA2020-04-29
X12+ and patient cable for the X12+ Telemeter with the following device name: PAT CBL 10WI recall (Z-1814-2020)WELCH ALLYN, INC/MORTARA2020-04-29
S4 and patient cable for the S4 Wireless Telemeter with the following device names: CABLE recall (Z-1815-2020)WELCH ALLYN, INC/MORTARA2020-04-29
Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor under the following dev recall (Z-1816-2020)WELCH ALLYN, INC/MORTARA2020-04-29
Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of real time ECG disp recall (Z-1817-2020)WELCH ALLYN, INC/MORTARA2020-04-29
Q-Tel. The Q-Tel RMS system is a computer-based cardiac and pulmonary rehabilitation data recall (Z-1818-2020)WELCH ALLYN, INC/MORTARA2020-04-29
Replaceable lead set for the Wireless Acquisition Module (WAM), which is the ECG front-end recall (Z-1819-2020)WELCH ALLYN, INC/MORTARA2020-04-29

Track WELCH ALLYN, INC/MORTARA automatically

Every clearance here is in the API, with alerts when new ones post.