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FDA 510(k)

MEDRAD ECOIL IMAGING SYSTEM FOR PHILIPS

K-Number: K063342 · 2006-11-30

ApplicantMedrad, Inc.
Decision Date2006-11-30
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDRAD ECOIL IMAGING SYSTEM FOR PHILIPS is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 2006-11-30 under 510(k) number K063342. 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 ECOIL IMAGING SYSTEM FOR PHILIPS?

MEDRAD ECOIL IMAGING SYSTEM FOR PHILIPS is a medical device that received FDA 510(k) clearance on 2006-11-30. The listed applicant is Medrad, Inc.. The 510(k) number is K063342.

When did MEDRAD ECOIL IMAGING SYSTEM FOR PHILIPS receive FDA 510(k) clearance?

MEDRAD ECOIL IMAGING SYSTEM FOR PHILIPS received FDA 510(k) clearance on 2006-11-30, under 510(k) number K063342.

Who is the listed applicant for MEDRAD ECOIL IMAGING SYSTEM FOR PHILIPS?

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 ECOIL IMAGING SYSTEM FOR PHILIPS?

The FDA product code for MEDRAD ECOIL IMAGING SYSTEM FOR PHILIPS 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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