Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Medline ReNewal Reprocesse
Surgical Instrument Service and Savings Inc.(Dba Medline Ren
Summary
Surgical Instrument Service and Savings Inc.(Dba Medline Ren received 510(k) clearance for Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Auto ID Technology (BD710DF282CT, BD710DF282RTS, BD710FJ282RTS, BD710FJ282CT), a NLH device. Cleared on 2024-11-15.
Details
Source
510(k) Clearance
External ID
K241224
Action Date
2024-11-15
Status
Traditional
Category
device
Product Code
NLH
Product Description
Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Auto ID Technology (BD710DF282CT, BD710DF282RTS, BD710FJ282RTS, BD710FJ282CT). Product code: NLH.
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.
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 Surgical Instrument Service and Savings Inc.(Dba Medline Ren have FDA actions?
This is the only FDA action we have on record for Surgical Instrument Service and Savings Inc.(Dba Medline Ren in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K241224" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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