Circon Acmi
Circon Acmi holds FDA 510(k) medical device clearances, first cleared 1988, most recent 2002.
Top product codes for Circon Acmi
Recent clearances by Circon Acmi
- K013165 — USA SERIES LAPAROSCOPES
- K980492 — AEH-3 ELECTROHYDRAULIC LITHOTRIPTER AND PROBES (E-1F, E-3F, E-5F, AND E-9F)
- K905705 — LAP 3501 HIGH FLOW INSUFFLATOR
- K905706 — GYN-1500 HYSTEROSCOPIC INUFFLATOR
- K884097 — MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES
- K884025 — CIRCON ACMI BICAP II THERAPEUTIC SYSTEM BC-200
- K884254 — CIRCON ACMI BICAP III THERAPEUTIC SYSTEM
- K884252 — CIRCON ACMI BICAP HEMORRHOID SYSTEM BH-10 & BHP-20
- K884306 — BICAP ABLATING FORCEPS BAF-7
- K883819 — BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P
Data sourced from openFDA. This site is unofficial and independent of the FDA.