ACCU-CHEK INSULIN PUMP CONFIGURATION SOFTWARE - Accu-Chek Insulin Pump Configuration Softwa
by Disetronic Medical Systems AG
510(k) K060876
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK060876 | Date15 Jun 2006 | StatusActive |
Recalls
-
- Terminated Z-1646-2009
The "up" and "down" buttons, which are used for changing the program in the menu or to administer additional insulin through a bolus delivery, may experience intermittent failure or completely cease to operate.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- LZG
- Models / Variants
- Accu-Chek Insulin Pump Configuration Softwa
- Device Class
- Class II
- Regulation
- 21 CFR Part 880.5725
- Advisory Committee
- General Hospital
- FDA Decision
- SESE Substantially Equivalent