GE 1.5T 8 CHANNEL TORSO COIL
K-Number: K031209 · 2003-05-23
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Device Summary
Frequently Asked Questions
What is the GE 1.5T 8 CHANNEL TORSO COIL?
GE 1.5T 8 CHANNEL TORSO COIL is a medical device that received FDA 510(k) clearance on 2003-05-23. The listed applicant is Ge Medical Systems, Inc.. The 510(k) number is K031209.
When did GE 1.5T 8 CHANNEL TORSO COIL receive FDA 510(k) clearance?
GE 1.5T 8 CHANNEL TORSO COIL received FDA 510(k) clearance on 2003-05-23, under 510(k) number K031209.
Who is the listed applicant for GE 1.5T 8 CHANNEL TORSO COIL?
The FDA 510(k) record lists Ge Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GE 1.5T 8 CHANNEL TORSO COIL?
The FDA product code for GE 1.5T 8 CHANNEL TORSO COIL is MOS.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Ge Medical Systems, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MOS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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