INNERWEAR, GENTLEMEN'S CHOICE W/NONOXYNOL-9
K-Number: K972429 · 1997-09-10
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Device Summary
Frequently Asked Questions
What is the INNERWEAR, GENTLEMEN'S CHOICE W/NONOXYNOL-9?
INNERWEAR, GENTLEMEN'S CHOICE W/NONOXYNOL-9 is a medical device that received FDA 510(k) clearance on 1997-09-10. The listed applicant is Custom Services Intl., Inc.. The 510(k) number is K972429.
When did INNERWEAR, GENTLEMEN'S CHOICE W/NONOXYNOL-9 receive FDA 510(k) clearance?
INNERWEAR, GENTLEMEN'S CHOICE W/NONOXYNOL-9 received FDA 510(k) clearance on 1997-09-10, under 510(k) number K972429.
Who is the listed applicant for INNERWEAR, GENTLEMEN'S CHOICE W/NONOXYNOL-9?
The FDA 510(k) record lists Custom Services Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INNERWEAR, GENTLEMEN'S CHOICE W/NONOXYNOL-9?
The FDA product code for INNERWEAR, GENTLEMEN'S CHOICE W/NONOXYNOL-9 is LTZ.
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 Custom Services Intl., 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: LTZ)
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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