Accu-Chek Softclix Blood Lancing System
Summary
Roche Diabetes Care, Inc. received 510(k) clearance for Accu-Chek Softclix Blood Lancing System, a QRL device. Cleared on 2022-02-17.
Details
Source
510(k) Clearance
External ID
K214022
Action Date
2022-02-17
Status
Traditional
Category
device
Product Code
QRL
Product Description
Accu-Chek Softclix Blood Lancing System. Product code: QRL.
Company
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Roche Diabetes Care, Inc. has received 7 total clearances in our database.
Roche Diabetes Care, Inc. has 13 FDA actions in our database, including 6 recalls and 7 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Roche Diabetes Care, Inc. have FDA actions?
Roche Diabetes Care, Inc. has 13 FDA actions in our database, including 6 recalls and 7 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K214022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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