3.0T TORSO PHASED ARRAY COIL
K-Number: K030495 · 2003-03-05
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Device Summary
Frequently Asked Questions
What is the 3.0T TORSO PHASED ARRAY COIL?
3.0T TORSO PHASED ARRAY COIL is a medical device that received FDA 510(k) clearance on 2003-03-05. The listed applicant is Ge Medical Systems, Inc.. The 510(k) number is K030495.
When did 3.0T TORSO PHASED ARRAY COIL receive FDA 510(k) clearance?
3.0T TORSO PHASED ARRAY COIL received FDA 510(k) clearance on 2003-03-05, under 510(k) number K030495.
Who is the listed applicant for 3.0T TORSO PHASED ARRAY 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 3.0T TORSO PHASED ARRAY COIL?
The FDA product code for 3.0T TORSO PHASED ARRAY 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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