FDA 510(k)

Z DEQ-II

K-Number: K973266 · 1997-09-23

Decision Date1997-09-23

Product CodeESD

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

Z DEQ-II is the device name listed in this FDA 510(k) record. The listed applicant is Electone, Inc.. It received FDA 510(k) clearance on 1997-09-23 under 510(k) number K973266. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Z DEQ-II?

Z DEQ-II is a medical device that received FDA 510(k) clearance on 1997-09-23. The listed applicant is Electone, Inc.. The 510(k) number is K973266.

When did Z DEQ-II receive FDA 510(k) clearance?

Z DEQ-II received FDA 510(k) clearance on 1997-09-23, under 510(k) number K973266.

Who is the listed applicant for Z DEQ-II?

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

What is the FDA product code for Z DEQ-II?

The FDA product code for Z DEQ-II is ESD.

Other records listing Electone, Inc. 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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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.