Caption Interpretation Automated Ejection Fraction Software
Summary
Caption Health received 510(k) clearance for Caption Interpretation Automated Ejection Fraction Software, a QIH device. Cleared on 2022-01-19.
Details
Source
510(k) Clearance
External ID
K210747
Action Date
2022-01-19
Status
Traditional
Category
device
Product Code
QIH
Product Description
Caption Interpretation Automated Ejection Fraction Software. Product code: QIH.
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.
Caption Health has 2 FDA actions in our database, including 1 recall and 1 clearance.
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 Caption Health have FDA actions?
Caption Health has 2 FDA actions in our database, including 1 recall and 1 device clearance.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K210747" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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