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FDA 510(k)

MRI PATIENT POSITIONING DEVICES

K-Number: K093738 · 2010-05-14

ApplicantMedtec, Inc.
Decision Date2010-05-14
Product CodeLNH
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 Medtec, Inc.. It received FDA 510(k) clearance on 2010-05-14 under 510(k) number K093738. The device is classified under product code LNH. 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 2010-05-14. The listed applicant is Medtec, Inc.. The 510(k) number is K093738.

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

MRI PATIENT POSITIONING DEVICES received FDA 510(k) clearance on 2010-05-14, under 510(k) number K093738.

Who is the listed applicant for MRI PATIENT POSITIONING DEVICES?

The FDA 510(k) record lists Medtec, 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 LNH.

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Other records listing Medtec, Inc. 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.

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Related Devices (Code: LNH)

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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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