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FDA 510(k)

CONCENTRACTORS

K-Number: K842114 · 1984-06-15

ApplicantAmox Corp.
Decision Date1984-06-15
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONCENTRACTORS is the device name listed in this FDA 510(k) record. The listed applicant is Amox Corp.. It received FDA 510(k) clearance on 1984-06-15 under 510(k) number K842114. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONCENTRACTORS?

CONCENTRACTORS is a medical device that received FDA 510(k) clearance on 1984-06-15. The listed applicant is Amox Corp.. The 510(k) number is K842114.

When did CONCENTRACTORS receive FDA 510(k) clearance?

CONCENTRACTORS received FDA 510(k) clearance on 1984-06-15, under 510(k) number K842114.

Who is the listed applicant for CONCENTRACTORS?

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

What is the FDA product code for CONCENTRACTORS?

The FDA product code for CONCENTRACTORS is CAW.

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Related Devices (Code: CAW)

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

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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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