SPEEDER 1.5T WRIST ARRAY COIL
K-Number: K072935 · 2007-10-31
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Device Summary
Frequently Asked Questions
What is the SPEEDER 1.5T WRIST ARRAY COIL?
SPEEDER 1.5T WRIST ARRAY COIL is a medical device that received FDA 510(k) clearance on 2007-10-31. The listed applicant is Quality Electrodynamics. The 510(k) number is K072935.
When did SPEEDER 1.5T WRIST ARRAY COIL receive FDA 510(k) clearance?
SPEEDER 1.5T WRIST ARRAY COIL received FDA 510(k) clearance on 2007-10-31, under 510(k) number K072935.
Who is the listed applicant for SPEEDER 1.5T WRIST ARRAY COIL?
The FDA 510(k) record lists Quality Electrodynamics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPEEDER 1.5T WRIST ARRAY COIL?
The FDA product code for SPEEDER 1.5T WRIST 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 Quality Electrodynamics 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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