Stellaris Elite vision enhancement system
Summary
Bausch and Lomb received 510(k) clearance for Stellaris Elite vision enhancement system, a HQC device. Cleared on 2024-02-26.
Details
Source
510(k) Clearance
External ID
K232084
Action Date
2024-02-26
Status
Traditional
Category
device
Product Code
HQC
Product Description
Stellaris Elite vision enhancement system. Product code: HQC.
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. Bausch and Lomb has received 2 total clearances in our database.
Bausch and Lomb has 6 FDA actions in our database, including 2 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 Bausch and Lomb have FDA actions?
Bausch and Lomb has 6 FDA actions in our database, including 0 recalls and 2 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K232084" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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