GREEN LOVE MALE CONTRACEPTIVE (CONDOM)
K-Number: K051842 · 2006-04-14
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Device Summary
Frequently Asked Questions
What is the GREEN LOVE MALE CONTRACEPTIVE (CONDOM)?
GREEN LOVE MALE CONTRACEPTIVE (CONDOM) is a medical device that received FDA 510(k) clearance on 2006-04-14. The listed applicant is Cupid Condom, Ltd.. The 510(k) number is K051842.
When did GREEN LOVE MALE CONTRACEPTIVE (CONDOM) receive FDA 510(k) clearance?
GREEN LOVE MALE CONTRACEPTIVE (CONDOM) received FDA 510(k) clearance on 2006-04-14, under 510(k) number K051842.
Who is the listed applicant for GREEN LOVE MALE CONTRACEPTIVE (CONDOM)?
The FDA 510(k) record lists Cupid Condom, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GREEN LOVE MALE CONTRACEPTIVE (CONDOM)?
The FDA product code for GREEN LOVE MALE CONTRACEPTIVE (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.
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
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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