F.M. Wiest USA, Inc.
FDA 510(k) medical device clearances.
Top product codes for F.M. Wiest USA, Inc.
Recent clearances by F.M. Wiest USA, Inc.
- K921871 — HYSTEROMAT(TM) 3700
- K920574 — CAMSYS 6300
- K920575 — MERKUR 4000
- K915751 — URETEROMAT 4400
- K911844 — HYSTEROFLATOR 1500
- K912071 — SPACE(TM) 7500
- K910883 — LAPAROFLATOR ELECTRONIC 3509
- K875137 — LAPAROFLATOR 3000, STANDARD AND ELECTRONIC
- K871180 — ARTHRO AUTOMAT 5002
- K871181 — ARTHROCOMBI 5003
- K865066 — ARTHROFLATOR
- K860571 — F.M. WEIST,KG (URODYNAMIC SYSTEMS)
Data sourced from openFDA. This site is unofficial and independent of the FDA.