PENTHOUSE CONDOMS
K-Number: K933153 · 1994-07-28
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Device Summary
Frequently Asked Questions
What is the PENTHOUSE CONDOMS?
PENTHOUSE CONDOMS is a medical device that received FDA 510(k) clearance on 1994-07-28. The listed applicant is Kuron Health Products Corp.. The 510(k) number is K933153.
When did PENTHOUSE CONDOMS receive FDA 510(k) clearance?
PENTHOUSE CONDOMS received FDA 510(k) clearance on 1994-07-28, under 510(k) number K933153.
Who is the listed applicant for PENTHOUSE CONDOMS?
The FDA 510(k) record lists Kuron Health Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PENTHOUSE CONDOMS?
The FDA product code for PENTHOUSE CONDOMS 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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