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FDA 510(k)

DYNACAD V1.0

K-Number: K041286 · 2004-07-21

ApplicantMri Devices Corp.
Decision Date2004-07-21
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DYNACAD V1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Mri Devices Corp.. It received FDA 510(k) clearance on 2004-07-21 under 510(k) number K041286. 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 DYNACAD V1.0?

DYNACAD V1.0 is a medical device that received FDA 510(k) clearance on 2004-07-21. The listed applicant is Mri Devices Corp.. The 510(k) number is K041286.

When did DYNACAD V1.0 receive FDA 510(k) clearance?

DYNACAD V1.0 received FDA 510(k) clearance on 2004-07-21, under 510(k) number K041286.

Who is the listed applicant for DYNACAD V1.0?

The FDA 510(k) record lists Mri Devices Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DYNACAD V1.0?

The FDA product code for DYNACAD V1.0 is LNH.

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Other records listing Mri Devices Corp. 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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