GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive Only; GEM Flex Coil 16-S Array, 3.0T
Summary
Shenzhen RF Tech Co., Ltd. received 510(k) clearance for GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive Only; GEM Flex Coil 16-S Array, 3.0T Receive Only, a MOS device. Cleared on 2026-04-01.
Details
Source
510(k) Clearance
External ID
K252876
Action Date
2026-04-01
Status
Traditional
Category
device
Product Code
MOS
Product Description
GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive Only; GEM Flex Coil 16-S Array, 3.0T Receive Only. Product code: MOS.
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. Shenzhen RF Tech Co., Ltd. has received 7 total clearances in our database.
Shenzhen RF Tech Co., Ltd. has 7 FDA actions in our database, including 7 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 Shenzhen RF Tech Co., Ltd. have FDA actions?
Shenzhen RF Tech Co., Ltd. has 7 FDA actions in our database, including 0 recalls and 7 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K252876" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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