Circon Acmi
Stamford, CT, US
Circon Acmi appears in FDA device records in Stamford, CT. FDA records list 10 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for Circon Acmi between 1988 and 2002. The busiest year on record is 1989, with 5. The most recent is 2002, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 1 |
| 1989 | 5 |
| 1991 | 2 |
| 1998 | 1 |
| 2002 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K013165 | USA SERIES LAPAROSCOPES | GCJ | Substantially Equivalent | |
| K980492 | AEH-3 ELECTROHYDRAULIC LITHOTRIPTER AND PROBES (E-1F, E-3F, E-5F, AND E-9F) | FFK | Substantially Equivalent | |
| K905706 | GYN-1500 HYSTEROSCOPIC INUFFLATOR | HIG | Substantially Equivalent | |
| K905705 | LAP 3501 HIGH FLOW INSUFFLATOR | HIF | Substantially Equivalent | |
| K884097 | MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES | ODC | Substantially Equivalent | |
| K884025 | CIRCON ACMI BICAP II THERAPEUTIC SYSTEM BC-200 | KNS | Substantially Equivalent | |
| K884254 | CIRCON ACMI BICAP III THERAPEUTIC SYSTEM | KNS | Substantially Equivalent | |
| K884252 | CIRCON ACMI BICAP HEMORRHOID SYSTEM BH-10 & BHP-20 | KNS | Substantially Equivalent | |
| K884306 | BICAP ABLATING FORCEPS BAF-7 | KNS | Substantially Equivalent | |
| K883819 | BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P | CCW | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain