Lipipor NLF1A Infusion Filter, Lipipor NLF2A & NLF2NTA Infusion Filters, Lipipor TNA2A Infusion Filter
Summary
Global Life Sciences Solutions USA, LLC received 510(k) clearance for Lipipor NLF1A Infusion Filter, Lipipor NLF2A & NLF2NTA Infusion Filters, Lipipor TNA2A Infusion Filter, a FPB device. Cleared on 2026-08-31.
Details
Source
510(k) Clearance
External ID
K261403
Action Date
2026-08-31
Status
Traditional
Category
device
Product Code
FPB
Product Description
Lipipor NLF1A Infusion Filter, Lipipor NLF2A & NLF2NTA Infusion Filters, Lipipor TNA2A Infusion Filter. Product code: FPB.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 445 device clearances issued this month.
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 Global Life Sciences Solutions USA, LLC have FDA actions?
This is the only FDA action we have on record for Global Life Sciences Solutions USA, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K261403" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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