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FDA 510(k)

CANAL AID

K-Number: K840165 · 1984-04-03

ApplicantQualitone
Decision Date1984-04-03
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CANAL AID is the device name listed in this FDA 510(k) record. The listed applicant is Qualitone. It received FDA 510(k) clearance on 1984-04-03 under 510(k) number K840165. 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 CANAL AID?

CANAL AID is a medical device that received FDA 510(k) clearance on 1984-04-03. The listed applicant is Qualitone. The 510(k) number is K840165.

When did CANAL AID receive FDA 510(k) clearance?

CANAL AID received FDA 510(k) clearance on 1984-04-03, under 510(k) number K840165.

Who is the listed applicant for CANAL AID?

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

What is the FDA product code for CANAL AID?

The FDA product code for CANAL AID 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.

Other records listing Qualitone 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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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

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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