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FDA 510(k)

MEDRAD 3.0T ECOIL IMAGING SYSTEM

K-Number: K060401 · 2006-03-15

ApplicantMedrad, Inc.
Decision Date2006-03-15
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDRAD 3.0T ECOIL IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 2006-03-15 under 510(k) number K060401. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDRAD 3.0T ECOIL IMAGING SYSTEM?

MEDRAD 3.0T ECOIL IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2006-03-15. The listed applicant is Medrad, Inc.. The 510(k) number is K060401.

When did MEDRAD 3.0T ECOIL IMAGING SYSTEM receive FDA 510(k) clearance?

MEDRAD 3.0T ECOIL IMAGING SYSTEM received FDA 510(k) clearance on 2006-03-15, under 510(k) number K060401.

Who is the listed applicant for MEDRAD 3.0T ECOIL IMAGING SYSTEM?

The FDA 510(k) record lists Medrad, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDRAD 3.0T ECOIL IMAGING SYSTEM?

The FDA product code for MEDRAD 3.0T ECOIL IMAGING SYSTEM is MOS.

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Related Devices (Code: MOS)

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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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