1.5T 16-CHANNEL HAND-WRIST COIL
K-Number: K103149 · 2011-01-03
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Device Summary
Frequently Asked Questions
What is the 1.5T 16-CHANNEL HAND-WRIST COIL?
1.5T 16-CHANNEL HAND-WRIST COIL is a medical device that received FDA 510(k) clearance on 2011-01-03. The listed applicant is Invivo Corporation. The 510(k) number is K103149.
When did 1.5T 16-CHANNEL HAND-WRIST COIL receive FDA 510(k) clearance?
1.5T 16-CHANNEL HAND-WRIST COIL received FDA 510(k) clearance on 2011-01-03, under 510(k) number K103149.
Who is the listed applicant for 1.5T 16-CHANNEL HAND-WRIST COIL?
The FDA 510(k) record lists Invivo Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 1.5T 16-CHANNEL HAND-WRIST COIL?
The FDA product code for 1.5T 16-CHANNEL HAND-WRIST 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 Invivo Corporation 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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