enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System
Summary
STERIS Corporation received 510(k) clearance for enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System, a FEB device. Cleared on 2024-12-02.
Details
Source
510(k) Clearance
External ID
K243433
Action Date
2024-12-02
Status
Special
Category
device
Product Code
FEB
Product Description
enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System. Product code: FEB.
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. STERIS Corporation has received 43 total clearances in our database.
STERIS Corporation has 71 FDA actions in our database, including 28 recalls and 43 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 STERIS Corporation have FDA actions?
STERIS Corporation has 71 FDA actions in our database, including 28 recalls and 43 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K243433" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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