Schiller, Ag

FDA Regulatory Profile

Summary

Total Recalls
2
510(k) Clearances
17
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2672-2025Class IIArgus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006August 8, 2025
Z-2734-2024Class IICARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570July 24, 2024

Recent 510(k) Clearances

K-NumberDeviceDate
K221056ARGUS PB-3000July 6, 2023
K183425CARDIOVIT AT-102 G2March 2, 2020
K170182CARDIOVIT FT-1July 19, 2017
K152043Diagnostic Station DS20May 6, 2016
K101619WELCH ALLYN 1500 PATIENT MONITORNovember 12, 2010
K063814BP-200 PLUSMarch 7, 2007
K053207ARGUS, MODEL LCMMay 19, 2006
K051368BR 102 PLUS BLOOD PRESSURE HOLTER SYSTEMAugust 9, 2005
K050686CARDIOVIT AT-10PLUSMay 4, 2005
K033738MONITORING SYSTEM, MODEL ARGUS PB-2200August 24, 2004
K031557CARDIOVIT AT-102April 14, 2004
K012226MONITORING SYSTEM,MODEL ARGUS PB-1000April 8, 2002
K992823SPIROVIT SP-2, PNEUMOCHECK IIMay 12, 2000
K984031SPIROVIT, MODEL SP-250April 30, 1999
K864465CARDIOVIT AT-6March 20, 1987
K850702CARDIOVIT CS-6 ECG-RECORDERApril 25, 1985
K841254CARDIOVIT CV-3January 24, 1985