MICROMRI WRIST COIL
K-Number: K073131 · 2008-01-18
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Device Summary
Frequently Asked Questions
What is the MICROMRI WRIST COIL?
MICROMRI WRIST COIL is a medical device that received FDA 510(k) clearance on 2008-01-18. The listed applicant is Micromri, Inc.. The 510(k) number is K073131.
When did MICROMRI WRIST COIL receive FDA 510(k) clearance?
MICROMRI WRIST COIL received FDA 510(k) clearance on 2008-01-18, under 510(k) number K073131.
Who is the listed applicant for MICROMRI WRIST COIL?
The FDA 510(k) record lists Micromri, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROMRI WRIST COIL?
The FDA product code for MICROMRI 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 Micromri, 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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