Schiller, Ag
FDA Regulatory Profile
Schiller, Ag appears in FDA public data with 2 recalls, 18 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-2672-2025, Class II) was initiated on Aug 8, 2025. Its most recent 510(k) clearance was granted on Aug 14, 2026.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 18
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-2672-2025 | Class II | Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006 | Aug 8, 2025 |
| Z-2734-2024 | Class II | CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570 | Jul 24, 2024 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K253562 | medilogFD | Aug 14, 2026 |
| K221056 | ARGUS PB-3000 | Jul 6, 2023 |
| K183425 | CARDIOVIT AT-102 G2 | Mar 2, 2020 |
| K170182 | CARDIOVIT FT-1 | Jul 19, 2017 |
| K152043 | Diagnostic Station DS20 | May 6, 2016 |
| K101619 | WELCH ALLYN 1500 PATIENT MONITOR | Nov 12, 2010 |
| K063814 | BP-200 PLUS | Mar 7, 2007 |
| K053207 | ARGUS, MODEL LCM | May 19, 2006 |
| K051368 | BR 102 PLUS BLOOD PRESSURE HOLTER SYSTEM | Aug 9, 2005 |
| K050686 | CARDIOVIT AT-10PLUS | May 4, 2005 |
| K033738 | MONITORING SYSTEM, MODEL ARGUS PB-2200 | Aug 24, 2004 |
| K031557 | CARDIOVIT AT-102 | Apr 14, 2004 |
| K012226 | MONITORING SYSTEM,MODEL ARGUS PB-1000 | Apr 8, 2002 |
| K992823 | SPIROVIT SP-2, PNEUMOCHECK II | May 12, 2000 |
| K984031 | SPIROVIT, MODEL SP-250 | Apr 30, 1999 |
| K864465 | CARDIOVIT AT-6 | Mar 20, 1987 |
| K850702 | CARDIOVIT CS-6 ECG-RECORDER | Apr 25, 1985 |
| K841254 | CARDIOVIT CV-3 | Jan 24, 1985 |