Flex and Loop Coil Set 1.5 T

FDA 510(k) K070629 · Siemens Medical Solutions

Substantially Equivalent

510(k) numberK070629

Submission

Device name
Flex and Loop Coil Set 1.5 T
Applicant
Siemens Medical Solutions
Erlangen, DE
Received
March 7, 2007
Decision date
March 26, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
MOS – Coil, Magnetic Resonance, Specialty
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1000
Specialty
Radiology

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K2609470.55T 12Ch Breast CoilMOS · Special Neocoil, LLC04/23/2026SE
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K252179GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive…MOS · Traditional Shenzhen RF Tech Co., Ltd.02/10/2026SE
K2537383.0T Air 32CH HnaMOS · Abbreviated Ge Healthcare Coils (Usa Instruments, Inc.)01/23/2026SE
K254190dS Base 1.5T; dS Base 3.0T; dS Head 1.5T; dS Head 3.0T; dS HeadNeck 1.5T; dS HeadNeck 3.0TMOS · Special Philips Medical Systems Nederland B.V.01/14/2026SE
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Questions and answers

When was Flex and Loop Coil Set 1.5 T cleared by the FDA?

Flex and Loop Coil Set 1.5 T (K070629) received a 510(k) decision of Substantially Equivalent on March 26, 2007, 19 days after the submission was received.

What is the product code of K070629?

The FDA product code is MOS – Coil, Magnetic Resonance, Specialty, a Class II (moderate risk) device regulated under 21 CFR 892.1000.