Acmi Corporation
FDA 510(k) & PMA Approved Devices — 16 products
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Total Devices16
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K061975 | PLASMASEAL OPEN FORCEPS, MODELS 2103PK AND 91701PK | GEI | 2006-08-10 | View |
| 510(k) | K060752 | ACMI DUR-HL LASER SYSTEMS | GEX | 2006-05-25 | View |
| 510(k) | K060269 | ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM | FBN | 2006-03-31 | View |
| 510(k) | K051593 | UROPASS URETERAL ACCESS SHEATH, MODEL 61224 | KNY | 2005-09-02 | View |
| 510(k) | K052044 | ACMI AUTOCLAVABLE URETEROSCOPE, MODELS MR-6A AND MR-6AL | FGB | 2005-08-16 | View |
| 510(k) | K043581 | DUAL LUMEN CATHETER | EYB | 2005-03-03 | View |
| 510(k) | K042069 | INVISIO IRL DIGITAL RIGID LAPAROSCOPE SYSTEM | GCJ | 2004-11-01 | View |
| 510(k) | K042225 | ACMI INVISIO ICN, MODELS ICN-0564 AND ICN-0565 | FAJ | 2004-09-10 | View |
| 510(k) | K031758 | ACMI M4 TELESCOPES | FBP | 2003-09-02 | View |
| 510(k) | K030960 | ECN ELECTRONIC VIDEO CYSTONEPHROSCOPE | FAJ | 2003-07-16 | View |
| 510(k) | K030935 | BERKELEY V-10 VACUUM CURETTAGE SYSTEM | HHI | 2003-06-23 | View |
| 510(k) | K030684 | SCOPE GUARD PROTECTIVE SHEATH, MODEL TEL-SH | OCU | 2003-06-03 | View |
| 510(k) | K031001 | ACMI VISTA CTR BIPOLAR LOOP ELECTRODE | FAS | 2003-05-21 | View |
| 510(k) | K023358 | USA SERIES DUR 8 ELITE, USA SERIES DUR 8, MODELS DUR 8E, DUR 8 | FGB | 2003-01-03 | View |
| 510(k) | K022480 | ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC | HIH | 2002-08-22 | View |
| 510(k) | K012018 | BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910 | GEI | 2002-07-16 | View |
No matching devices.
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