1.0T 8-CHANNEL PANORAMA BREAST ARRAY COIL
K-Number: K093284 · 2010-02-01
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Device Summary
Frequently Asked Questions
What is the 1.0T 8-CHANNEL PANORAMA BREAST ARRAY COIL?
1.0T 8-CHANNEL PANORAMA BREAST ARRAY COIL is a medical device that received FDA 510(k) clearance on 2010-02-01. The listed applicant is Invivo Corporation. The 510(k) number is K093284.
When did 1.0T 8-CHANNEL PANORAMA BREAST ARRAY COIL receive FDA 510(k) clearance?
1.0T 8-CHANNEL PANORAMA BREAST ARRAY COIL received FDA 510(k) clearance on 2010-02-01, under 510(k) number K093284.
Who is the listed applicant for 1.0T 8-CHANNEL PANORAMA BREAST ARRAY COIL?
The FDA 510(k) record lists Invivo Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 1.0T 8-CHANNEL PANORAMA BREAST ARRAY COIL?
The FDA product code for 1.0T 8-CHANNEL PANORAMA BREAST 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 Invivo Corporation 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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