Acmi Corporation
Acmi Corporation holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2006.
Top product codes for Acmi Corporation
- FAJ — Gastroenterology, Urology
- FGB — Gastroenterology, Urology
- GEI — General, Plastic Surgery
- EYB — Gastroenterology, Urology
- FAS — Gastroenterology, Urology
- FBN — Gastroenterology, Urology
- FBP — Gastroenterology, Urology
- GCJ — Gastroenterology, Urology
- GEX — General, Plastic Surgery
- HHI — Obstetrics/Gynecology
Recent clearances by Acmi Corporation
- K061975 — PLASMASEAL OPEN FORCEPS, MODELS 2103PK AND 91701PK
- K060752 — ACMI DUR-HL LASER SYSTEMS
- K060269 — ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM
- K051593 — UROPASS URETERAL ACCESS SHEATH, MODEL 61224
- K052044 — ACMI AUTOCLAVABLE URETEROSCOPE, MODELS MR-6A AND MR-6AL
- K043581 — DUAL LUMEN CATHETER
- K042069 — INVISIO IRL DIGITAL RIGID LAPAROSCOPE SYSTEM
- K042225 — ACMI INVISIO ICN, MODELS ICN-0564 AND ICN-0565
- K031758 — ACMI M4 TELESCOPES
- K030960 — ECN ELECTRONIC VIDEO CYSTONEPHROSCOPE
- K030935 — BERKELEY V-10 VACUUM CURETTAGE SYSTEM
- K030684 — SCOPE GUARD PROTECTIVE SHEATH, MODEL TEL-SH
- K031001 — ACMI VISTA CTR BIPOLAR LOOP ELECTRODE
- K023358 — USA SERIES DUR 8 ELITE, USA SERIES DUR 8, MODELS DUR 8E, DUR 8
- K022480 — ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC
- K012018 — BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910
Data sourced from openFDA. This site is unofficial and independent of the FDA.