Otsuka Digital Feedback Device
Summary
Otsuka America Pharmaceutical, Inc. received 510(k) clearance for Otsuka Digital Feedback Device, a OZW device. Cleared on 2025-06-30.
Details
Source
510(k) Clearance
External ID
K251088
Action Date
2025-06-30
Status
Traditional
Category
device
Product Code
OZW
Product Description
Otsuka Digital Feedback Device. Product code: OZW.
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. Otsuka America Pharmaceutical, Inc. has received 3 total clearances in our database.
Otsuka America Pharmaceutical, Inc. has 3 FDA actions in our database, including 3 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 Otsuka America Pharmaceutical, Inc. have FDA actions?
Otsuka America Pharmaceutical, Inc. has 3 FDA actions in our database, including 0 recalls and 3 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K251088" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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