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FDA 510(k)

TROJAN FOR WOMEN

K-Number: K890863 · 1989-04-04

ApplicantArmkel, LLC
Decision Date1989-04-04
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROJAN FOR WOMEN is the device name listed in this FDA 510(k) record. The listed applicant is Armkel, LLC. It received FDA 510(k) clearance on 1989-04-04 under 510(k) number K890863. The device is classified under product code HIS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROJAN FOR WOMEN?

TROJAN FOR WOMEN is a medical device that received FDA 510(k) clearance on 1989-04-04. The listed applicant is Armkel, LLC. The 510(k) number is K890863.

When did TROJAN FOR WOMEN receive FDA 510(k) clearance?

TROJAN FOR WOMEN received FDA 510(k) clearance on 1989-04-04, under 510(k) number K890863.

Who is the listed applicant for TROJAN FOR WOMEN?

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 FOR WOMEN?

The FDA product code for TROJAN FOR WOMEN is HIS.

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Related Devices (Code: HIS)

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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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