Wellead® Hydrophilic Intermittent Catheter Ready to Use; Wellead® Hydrophilic Intermittent Catheter Compact
Summary
Well Lead Medical Co., Ltd. received 510(k) clearance for Wellead® Hydrophilic Intermittent Catheter Ready to Use; Wellead® Hydrophilic Intermittent Catheter Compact, a GBM device. Cleared on 2025-03-05.
Details
Source
510(k) Clearance
External ID
K241734
Action Date
2025-03-05
Status
Traditional
Category
device
Product Code
GBM
Product Description
Wellead® Hydrophilic Intermittent Catheter Ready to Use; Wellead® Hydrophilic Intermittent Catheter Compact. Product code: GBM.
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. Well Lead Medical Co., Ltd. has received 5 total clearances in our database.
Well Lead Medical Co., Ltd. has 5 FDA actions in our database, including 5 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 Well Lead Medical Co., Ltd. have FDA actions?
Well Lead Medical Co., Ltd. has 5 FDA actions in our database, including 0 recalls and 5 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K241734" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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