MODEL 455GE PHASED ARRAY WRIST COIL
K-Number: K010074 · 2001-04-03
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Device Summary
Frequently Asked Questions
What is the MODEL 455GE PHASED ARRAY WRIST COIL?
MODEL 455GE PHASED ARRAY WRIST COIL is a medical device that received FDA 510(k) clearance on 2001-04-03. The listed applicant is Medical Advances, Inc.. The 510(k) number is K010074.
When did MODEL 455GE PHASED ARRAY WRIST COIL receive FDA 510(k) clearance?
MODEL 455GE PHASED ARRAY WRIST COIL received FDA 510(k) clearance on 2001-04-03, under 510(k) number K010074.
Who is the listed applicant for MODEL 455GE PHASED ARRAY WRIST COIL?
The FDA 510(k) record lists Medical Advances, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 455GE PHASED ARRAY WRIST COIL?
The FDA product code for MODEL 455GE PHASED ARRAY 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 Medical Advances, 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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