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FDA 510(k)

MRI PATIENT POSITIONING DEVICES

K-Number: K080072 · 2008-06-04

ApplicantCIVCO Medical Instruments Co., Inc.
Decision Date2008-06-04
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRI PATIENT POSITIONING DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is CIVCO Medical Instruments Co., Inc.. It received FDA 510(k) clearance on 2008-06-04 under 510(k) number K080072. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MRI PATIENT POSITIONING DEVICES?

MRI PATIENT POSITIONING DEVICES is a medical device that received FDA 510(k) clearance on 2008-06-04. The listed applicant is CIVCO Medical Instruments Co., Inc.. The 510(k) number is K080072.

When did MRI PATIENT POSITIONING DEVICES receive FDA 510(k) clearance?

MRI PATIENT POSITIONING DEVICES received FDA 510(k) clearance on 2008-06-04, under 510(k) number K080072.

Who is the listed applicant for MRI PATIENT POSITIONING DEVICES?

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

What is the FDA product code for MRI PATIENT POSITIONING DEVICES?

The FDA product code for MRI PATIENT POSITIONING DEVICES is IYE.

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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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