Accu-Chek Pocket Compass Diabetes Management Software
FDA 510(k) K050760 · Roche Diagnostics Corp.
510(k) numberK050760
Submission
- Device name
- Accu-Chek Pocket Compass Diabetes Management Software
- Applicant
- Roche Diagnostics Corp.
Indianapolis, IN, US - Received
- March 24, 2005
- Decision date
- September 13, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- LZG – Pump, Infusion, Insulin
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5725
- Specialty
- General Hospital
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Questions and answers
When was Accu-Chek Pocket Compass Diabetes Management Software cleared by the FDA?
Accu-Chek Pocket Compass Diabetes Management Software (K050760) received a 510(k) decision of Substantially Equivalent on September 13, 2005, 173 days after the submission was received.
What is the product code of K050760?
The FDA product code is LZG – Pump, Infusion, Insulin, a Class II (moderate risk) device regulated under 21 CFR 880.5725.