MALE NATURAL RUBBER LATEX CONDOM
K-Number: K050244 · 2005-04-08
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Device Summary
Frequently Asked Questions
What is the MALE NATURAL RUBBER LATEX CONDOM?
MALE NATURAL RUBBER LATEX CONDOM is a medical device that received FDA 510(k) clearance on 2005-04-08. The listed applicant is Nrs Global Partners. The 510(k) number is K050244.
When did MALE NATURAL RUBBER LATEX CONDOM receive FDA 510(k) clearance?
MALE NATURAL RUBBER LATEX CONDOM received FDA 510(k) clearance on 2005-04-08, under 510(k) number K050244.
Who is the listed applicant for MALE NATURAL RUBBER LATEX CONDOM?
The FDA 510(k) record lists Nrs Global Partners as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MALE NATURAL RUBBER LATEX CONDOM?
The FDA product code for MALE NATURAL RUBBER LATEX 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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