6 CHANNEL BODY COIL
K-Number: K023571 · 2002-11-20
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Device Summary
Frequently Asked Questions
What is the 6 CHANNEL BODY COIL?
6 CHANNEL BODY COIL is a medical device that received FDA 510(k) clearance on 2002-11-20. The listed applicant is Siemens Medical Systems, Inc.. The 510(k) number is K023571.
When did 6 CHANNEL BODY COIL receive FDA 510(k) clearance?
6 CHANNEL BODY COIL received FDA 510(k) clearance on 2002-11-20, under 510(k) number K023571.
Who is the listed applicant for 6 CHANNEL BODY COIL?
The FDA 510(k) record lists Siemens Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 6 CHANNEL BODY COIL?
The FDA product code for 6 CHANNEL BODY 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 Siemens 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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