F.M. Wiest USA, Inc.
F.M. Wiest USA, Inc. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 1994.
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.