The following data is part of a premarket notification filed by Cane S.r.l. with the FDA for Crono And Crono, Model 30.
Device ID | K041414 |
510k Number | K041414 |
Device Name: | CRONO AND CRONO, MODEL 30 |
Classification | Pump, Infusion |
Applicant | CANE S.R.L. P.O. BOX 7007 Deerfield, IL 60015 |
Contact | Daniel Kamm |
Correspondent | Daniel Kamm CANE S.R.L. P.O. BOX 7007 Deerfield, IL 60015 |
Product Code | FRN |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-05-27 |
Decision Date | 2004-07-08 |
Summary: | summary |