Zenition 90
Summary
Philips Medical Systems Nederlands B.V. received 510(k) clearance for Zenition 90, a OWB device. Cleared on 2024-05-22.
Details
Source
510(k) Clearance
External ID
K240224
Action Date
2024-05-22
Status
Abbreviated
Category
device
Product Code
OWB
Product Description
Zenition 90. Product code: OWB.
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. Philips Medical Systems Nederlands B.V. has received 2 total clearances in our database.
Philips Medical Systems Nederlands B.V. has 2 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 Philips Medical Systems Nederlands B.V. have FDA actions?
Philips Medical Systems Nederlands B.V. has 2 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 "K240224" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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