Schiller AG
FDA 510(k) medical device clearances.
Top product codes for Schiller AG
Recent clearances by Schiller AG
- 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.