LONG LOVE CONDOM
K-Number: K033541 · 2003-12-23
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Device Summary
Frequently Asked Questions
What is the LONG LOVE CONDOM?
LONG LOVE CONDOM is a medical device that received FDA 510(k) clearance on 2003-12-23. The listed applicant is Unidus Corp.. The 510(k) number is K033541.
When did LONG LOVE CONDOM receive FDA 510(k) clearance?
LONG LOVE CONDOM received FDA 510(k) clearance on 2003-12-23, under 510(k) number K033541.
Who is the listed applicant for LONG LOVE CONDOM?
The FDA 510(k) record lists Unidus Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LONG LOVE CONDOM?
The FDA product code for LONG LOVE 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 Unidus Corp. 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
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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