MICROLET NEXT lancing device, MICROLET Lancet— 510(k) K220633
Substantially EquivalentAscensia Diabetes Care U.S., Inc.
FDA 510(k) clearance K220633 for MICROLET NEXT lancing device, MICROLET Lancet, Substantially Equivalent on 2022-06-03. Applicant: Ascensia Diabetes Care U.S., Inc..
Clearance details
- Applicant
- Ascensia Diabetes Care U.S., Inc.
- Product code
- Code QRL
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Parsippany, NJ, US
Adverse events under product code QRL
product code QRL- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.