Schiller AG
Schiller AG holds FDA 510(k) medical device clearances, first cleared 1985, most recent 2026, with 2 FDA device recalls on record.
Top product codes for Schiller AG
FDA recalls by Schiller AG
- Z-2672-2025 — Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
- Z-2734-2024 — CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Schiller AG
- K253562 — medilogFD
- K221056 — ARGUS PB-3000
- K183425 — CARDIOVIT AT-102 G2
- K170182 — CARDIOVIT FT-1
- K152043 — Diagnostic Station DS20
- K101619 — WELCH ALLYN 1500 PATIENT MONITOR
- K063814 — BP-200 PLUS
- K053207 — ARGUS, MODEL LCM
- K051368 — BR 102 PLUS BLOOD PRESSURE HOLTER SYSTEM
- K050686 — CARDIOVIT AT-10PLUS
- K033738 — MONITORING SYSTEM, MODEL ARGUS PB-2200
- K031557 — CARDIOVIT AT-102
- K012226 — MONITORING SYSTEM,MODEL ARGUS PB-1000
- K992823 — SPIROVIT SP-2, PNEUMOCHECK II
- K984031 — SPIROVIT, MODEL SP-250
- K850702 — CARDIOVIT CS-6 ECG-RECORDER
- K841254 — CARDIOVIT CV-3
Data sourced from openFDA. This site is unofficial and independent of the FDA.