1.5T 32-CHANNEL HEAD COIL AND 3T 32-CHANNEL HEAD COIL
K-Number: K072909 · 2007-10-31
Advertisement
Device Summary
Frequently Asked Questions
What is the 1.5T 32-CHANNEL HEAD COIL AND 3T 32-CHANNEL HEAD COIL?
1.5T 32-CHANNEL HEAD COIL AND 3T 32-CHANNEL HEAD COIL is a medical device that received FDA 510(k) clearance on 2007-10-31. The listed applicant is Siemens AG Medical Solutions. The 510(k) number is K072909.
When did 1.5T 32-CHANNEL HEAD COIL AND 3T 32-CHANNEL HEAD COIL receive FDA 510(k) clearance?
1.5T 32-CHANNEL HEAD COIL AND 3T 32-CHANNEL HEAD COIL received FDA 510(k) clearance on 2007-10-31, under 510(k) number K072909.
Who is the listed applicant for 1.5T 32-CHANNEL HEAD COIL AND 3T 32-CHANNEL HEAD COIL?
The FDA 510(k) record lists Siemens AG Medical Solutions as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 1.5T 32-CHANNEL HEAD COIL AND 3T 32-CHANNEL HEAD COIL?
The FDA product code for 1.5T 32-CHANNEL HEAD COIL AND 3T 32-CHANNEL HEAD 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 Siemens AG Medical Solutions 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.
Advertisement