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FDA 510(k)

MATRIX STRIP, DEAD-SOFT

K-Number: K772316 · 1978-01-03

ApplicantDen-Mat Corp.
Decision Date1978-01-03
Product CodeDZN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MATRIX STRIP, DEAD-SOFT is the device name listed in this FDA 510(k) record. The listed applicant is Den-Mat Corp.. It received FDA 510(k) clearance on 1978-01-03 under 510(k) number K772316. The device is classified under product code DZN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRIX STRIP, DEAD-SOFT?

MATRIX STRIP, DEAD-SOFT is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Den-Mat Corp.. The 510(k) number is K772316.

When did MATRIX STRIP, DEAD-SOFT receive FDA 510(k) clearance?

MATRIX STRIP, DEAD-SOFT received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772316.

Who is the listed applicant for MATRIX STRIP, DEAD-SOFT?

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

What is the FDA product code for MATRIX STRIP, DEAD-SOFT?

The FDA product code for MATRIX STRIP, DEAD-SOFT is DZN.

Related Clinical Trials

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.

Other records listing Den-Mat 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.

View all 29 devices →

Related Devices (Code: DZN)

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.

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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