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FDA 510(k)

QCC CUSTOM CANAL AND QE1 ALL ITE

K-Number: K920911 · 1992-04-27

Decision Date1992-04-27
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

QCC CUSTOM CANAL AND QE1 ALL ITE is the device name listed in this FDA 510(k) record. The listed applicant is Qualitech Electronics, Inc.. It received FDA 510(k) clearance on 1992-04-27 under 510(k) number K920911. 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 QCC CUSTOM CANAL AND QE1 ALL ITE?

QCC CUSTOM CANAL AND QE1 ALL ITE is a medical device that received FDA 510(k) clearance on 1992-04-27. The listed applicant is Qualitech Electronics, Inc.. The 510(k) number is K920911.

When did QCC CUSTOM CANAL AND QE1 ALL ITE receive FDA 510(k) clearance?

QCC CUSTOM CANAL AND QE1 ALL ITE received FDA 510(k) clearance on 1992-04-27, under 510(k) number K920911.

Who is the listed applicant for QCC CUSTOM CANAL AND QE1 ALL ITE?

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

What is the FDA product code for QCC CUSTOM CANAL AND QE1 ALL ITE?

The FDA product code for QCC CUSTOM CANAL AND QE1 ALL ITE is ESD.

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.

Related Devices (Code: ESD)

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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