CROSSLEAD Tracker
Summary
Asahi Intecc Co., Ltd. received 510(k) clearance for CROSSLEAD Tracker, a DQX device. Cleared on 2024-08-14.
Details
Source
510(k) Clearance
External ID
K241510
Action Date
2024-08-14
Status
Special
Category
device
Product Code
DQX
Product Description
CROSSLEAD Tracker. Product code: DQX.
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. Asahi Intecc Co., Ltd. has received 18 total clearances in our database.
Asahi Intecc Co., Ltd. has 18 FDA actions in our database, including 18 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 Asahi Intecc Co., Ltd. have FDA actions?
Asahi Intecc Co., Ltd. has 18 FDA actions in our database, including 0 recalls and 18 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K241510" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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