G-SCAN CERVICAL SPINE COIL
K-Number: K052077 · 2005-08-16
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Device Summary
Frequently Asked Questions
What is the G-SCAN CERVICAL SPINE COIL?
G-SCAN CERVICAL SPINE COIL is a medical device that received FDA 510(k) clearance on 2005-08-16. The listed applicant is Esaote, S.p.A.. The 510(k) number is K052077.
When did G-SCAN CERVICAL SPINE COIL receive FDA 510(k) clearance?
G-SCAN CERVICAL SPINE COIL received FDA 510(k) clearance on 2005-08-16, under 510(k) number K052077.
Who is the listed applicant for G-SCAN CERVICAL SPINE COIL?
The FDA 510(k) record lists Esaote, S.p.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for G-SCAN CERVICAL SPINE COIL?
The FDA product code for G-SCAN CERVICAL SPINE 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 Esaote, S.p.A. 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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