PowerWire® 14 Radiofrequency Guidewire Kit
Summary
Baylis Medical Technologies, Inc. received 510(k) clearance for PowerWire® 14 Radiofrequency Guidewire Kit, a PDU device. Cleared on 2025-09-11.
Details
Source
510(k) Clearance
External ID
K251158
Action Date
2025-09-11
Status
Traditional
Category
device
Product Code
PDU
Product Description
PowerWire® 14 Radiofrequency Guidewire Kit. Product code: PDU.
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. Baylis Medical Technologies, Inc. has received 4 total clearances in our database.
Baylis Medical Technologies, Inc. has 4 FDA actions in our database, including 4 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 Baylis Medical Technologies, Inc. have FDA actions?
Baylis Medical Technologies, Inc. has 4 FDA actions in our database, including 0 recalls and 4 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K251158" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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