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FDA 510(k)

DYNATRAC

K-Number: K872974 · 1987-11-23

ApplicantMed*Ex Diagnostics of Canada, Inc.
Decision Date1987-11-23
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DYNATRAC is the device name listed in this FDA 510(k) record. The listed applicant is Med*Ex Diagnostics of Canada, Inc.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K872974. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNATRAC?

DYNATRAC is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Med*Ex Diagnostics of Canada, Inc.. The 510(k) number is K872974.

When did DYNATRAC receive FDA 510(k) clearance?

DYNATRAC received FDA 510(k) clearance on 1987-11-23, under 510(k) number K872974.

Who is the listed applicant for DYNATRAC?

The FDA 510(k) record lists Med*Ex Diagnostics of Canada, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DYNATRAC?

The FDA product code for DYNATRAC is IPF.

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Related Devices (Code: IPF)

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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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