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FDA 510(k)

TROJAN CRYSTAL CLEAR LIQUID

K-Number: K013614 · 2002-02-01

ApplicantArmkel, LLC
Decision Date2002-02-01
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROJAN CRYSTAL CLEAR LIQUID is the device name listed in this FDA 510(k) record. The listed applicant is Armkel, LLC. It received FDA 510(k) clearance on 2002-02-01 under 510(k) number K013614. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROJAN CRYSTAL CLEAR LIQUID?

TROJAN CRYSTAL CLEAR LIQUID is a medical device that received FDA 510(k) clearance on 2002-02-01. The listed applicant is Armkel, LLC. The 510(k) number is K013614.

When did TROJAN CRYSTAL CLEAR LIQUID receive FDA 510(k) clearance?

TROJAN CRYSTAL CLEAR LIQUID received FDA 510(k) clearance on 2002-02-01, under 510(k) number K013614.

Who is the listed applicant for TROJAN CRYSTAL CLEAR LIQUID?

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 TROJAN CRYSTAL CLEAR LIQUID?

The FDA product code for TROJAN CRYSTAL CLEAR LIQUID is NUC.

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Related Devices (Code: NUC)

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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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