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FDA 510(k)

CRACK DETECTOR, DEN-MAT

K-Number: K770492 · 1977-03-21

ApplicantDey-Mat, Inc.
Decision Date1977-03-21
Product CodeEFH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CRACK DETECTOR, DEN-MAT is the device name listed in this FDA 510(k) record. The listed applicant is Dey-Mat, Inc.. It received FDA 510(k) clearance on 1977-03-21 under 510(k) number K770492. The device is classified under product code EFH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRACK DETECTOR, DEN-MAT?

CRACK DETECTOR, DEN-MAT is a medical device that received FDA 510(k) clearance on 1977-03-21. The listed applicant is Dey-Mat, Inc.. The 510(k) number is K770492.

When did CRACK DETECTOR, DEN-MAT receive FDA 510(k) clearance?

CRACK DETECTOR, DEN-MAT received FDA 510(k) clearance on 1977-03-21, under 510(k) number K770492.

Who is the listed applicant for CRACK DETECTOR, DEN-MAT?

The FDA 510(k) record lists Dey-Mat, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRACK DETECTOR, DEN-MAT?

The FDA product code for CRACK DETECTOR, DEN-MAT is EFH.

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Related Devices (Code: EFH)

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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