FloNavi Open Field Fluorescence Imaging System
Summary
Guangdong Optomedic Technologies, Inc. received 510(k) clearance for FloNavi Open Field Fluorescence Imaging System, a OWN device. Cleared on 2023-07-17.
Details
Source
510(k) Clearance
External ID
K230407
Action Date
2023-07-17
Status
Traditional
Category
device
Product Code
OWN
Product Description
FloNavi Open Field Fluorescence Imaging System. Product code: OWN.
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. Guangdong Optomedic Technologies, Inc. has received 8 total clearances in our database.
Guangdong Optomedic Technologies, Inc. has 8 FDA actions in our database, including 8 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 Guangdong Optomedic Technologies, Inc. have FDA actions?
Guangdong Optomedic Technologies, Inc. has 8 FDA actions in our database, including 0 recalls and 8 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K230407" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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