HybridTherm System
Summary
Erbe Elektromedizin GmbH received 510(k) clearance for HybridTherm System, a GEI device. Cleared on 2024-08-05.
Details
Source
510(k) Clearance
External ID
K240932
Action Date
2024-08-05
Status
Traditional
Category
device
Product Code
GEI
Product Description
HybridTherm System. Product code: GEI.
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. Erbe Elektromedizin GmbH has received 10 total clearances in our database.
Erbe Elektromedizin GmbH has 10 FDA actions in our database, including 10 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 Erbe Elektromedizin GmbH have FDA actions?
Erbe Elektromedizin GmbH has 10 FDA actions in our database, including 0 recalls and 10 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K240932" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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