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FDA 510(k)

ACCOR MATRIX

K-Number: K790633 · 1979-05-17

ApplicantAccor, Inc.
Decision Date1979-05-17
Product CodeDZN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACCOR MATRIX is the device name listed in this FDA 510(k) record. The listed applicant is Accor, Inc.. It received FDA 510(k) clearance on 1979-05-17 under 510(k) number K790633. 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 ACCOR MATRIX?

ACCOR MATRIX is a medical device that received FDA 510(k) clearance on 1979-05-17. The listed applicant is Accor, Inc.. The 510(k) number is K790633.

When did ACCOR MATRIX receive FDA 510(k) clearance?

ACCOR MATRIX received FDA 510(k) clearance on 1979-05-17, under 510(k) number K790633.

Who is the listed applicant for ACCOR MATRIX?

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

What is the FDA product code for ACCOR MATRIX?

The FDA product code for ACCOR MATRIX is DZN.

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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.

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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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