FLEXICOIL - MALLEABLE RECEIVE-ONLY SURFACE COIL
K-Number: K020601 · 2002-04-24
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Device Summary
Frequently Asked Questions
What is the FLEXICOIL - MALLEABLE RECEIVE-ONLY SURFACE COIL?
FLEXICOIL - MALLEABLE RECEIVE-ONLY SURFACE COIL is a medical device that received FDA 510(k) clearance on 2002-04-24. The listed applicant is Odin Medical Technologies , Ltd.. The 510(k) number is K020601.
When did FLEXICOIL - MALLEABLE RECEIVE-ONLY SURFACE COIL receive FDA 510(k) clearance?
FLEXICOIL - MALLEABLE RECEIVE-ONLY SURFACE COIL received FDA 510(k) clearance on 2002-04-24, under 510(k) number K020601.
Who is the listed applicant for FLEXICOIL - MALLEABLE RECEIVE-ONLY SURFACE COIL?
The FDA 510(k) record lists Odin Medical Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXICOIL - MALLEABLE RECEIVE-ONLY SURFACE COIL?
The FDA product code for FLEXICOIL - MALLEABLE RECEIVE-ONLY SURFACE 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 Odin Medical Technologies , Ltd. 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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