The following data is part of a premarket notification filed by Cane S.r.l. with the FDA for Crono Go..
| Device ID | K052219 |
| 510k Number | K052219 |
| Device Name: | CRONO GO. |
| Classification | Pump, Infusion |
| Applicant | CANE S.R.L. VIA PAVIA, 105/I Rivoli-cascine Vica (torino), IT 10090 |
| Contact | Carlo Musso |
| Correspondent | Carlo Musso CANE S.R.L. VIA PAVIA, 105/I Rivoli-cascine Vica (torino), IT 10090 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-08-15 |
| Decision Date | 2005-09-13 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08050616612052 | K052219 | 000 |