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FDA 510(k)

LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM

K-Number: K001883 · 2000-07-31

Decision Date2000-07-31
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM is the device name listed in this FDA 510(k) record. The listed applicant is Ansell Healthcare, Inc.. It received FDA 510(k) clearance on 2000-07-31 under 510(k) number K001883. 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 LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM?

LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM is a medical device that received FDA 510(k) clearance on 2000-07-31. The listed applicant is Ansell Healthcare, Inc.. The 510(k) number is K001883.

When did LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM receive FDA 510(k) clearance?

LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM received FDA 510(k) clearance on 2000-07-31, under 510(k) number K001883.

Who is the listed applicant for LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM?

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

What is the FDA product code for LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM?

The FDA product code for LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM is HIS.

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 Ansell Healthcare, Inc. 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.

Related Devices (Code: HIS)

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

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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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