MODEL EXS-63-INT SMALL EXTREMITY ARRAY COIL
K-Number: K022487 · 2002-08-23
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Device Summary
Frequently Asked Questions
What is the MODEL EXS-63-INT SMALL EXTREMITY ARRAY COIL?
MODEL EXS-63-INT SMALL EXTREMITY ARRAY COIL is a medical device that received FDA 510(k) clearance on 2002-08-23. The listed applicant is Mri Devices Corp.. The 510(k) number is K022487.
When did MODEL EXS-63-INT SMALL EXTREMITY ARRAY COIL receive FDA 510(k) clearance?
MODEL EXS-63-INT SMALL EXTREMITY ARRAY COIL received FDA 510(k) clearance on 2002-08-23, under 510(k) number K022487.
Who is the listed applicant for MODEL EXS-63-INT SMALL EXTREMITY ARRAY COIL?
The FDA 510(k) record lists Mri Devices Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL EXS-63-INT SMALL EXTREMITY ARRAY COIL?
The FDA product code for MODEL EXS-63-INT SMALL EXTREMITY 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 Mri Devices Corp. 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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