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FDA 510(k)

ANATON

K-Number: K801046 · 1980-05-14

ApplicantArmkel, LLC
Decision Date1980-05-14
Product CodeDHN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ANATON is the device name listed in this FDA 510(k) record. The listed applicant is Armkel, LLC. It received FDA 510(k) clearance on 1980-05-14 under 510(k) number K801046. The device is classified under product code DHN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANATON?

ANATON is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is Armkel, LLC. The 510(k) number is K801046.

When did ANATON receive FDA 510(k) clearance?

ANATON received FDA 510(k) clearance on 1980-05-14, under 510(k) number K801046.

Who is the listed applicant for ANATON?

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

What is the FDA product code for ANATON?

The FDA product code for ANATON is DHN.

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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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