AccurSound Electronic Stethoscope AS-101
Summary
Heroic Faith International , Ltd. received 510(k) clearance for AccurSound Electronic Stethoscope AS-101, a DQD device. Cleared on 2023-03-23.
Details
Source
510(k) Clearance
External ID
K221805
Action Date
2023-03-23
Status
Traditional
Category
device
Product Code
DQD
Product Description
AccurSound Electronic Stethoscope AS-101. Product code: DQD.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 389 device clearances issued this month. Heroic Faith International , Ltd. has received 3 total clearances in our database.
Heroic Faith International , Ltd. 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 Heroic Faith International , Ltd. have FDA actions?
Heroic Faith International , Ltd. 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 "K221805" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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