KOTEX PROFILE SHAPED MAXI PAD
K-Number: K871210 · 1987-04-10
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Device Summary
Frequently Asked Questions
What is the KOTEX PROFILE SHAPED MAXI PAD?
KOTEX PROFILE SHAPED MAXI PAD is a medical device that received FDA 510(k) clearance on 1987-04-10. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K871210.
When did KOTEX PROFILE SHAPED MAXI PAD receive FDA 510(k) clearance?
KOTEX PROFILE SHAPED MAXI PAD received FDA 510(k) clearance on 1987-04-10, under 510(k) number K871210.
Who is the listed applicant for KOTEX PROFILE SHAPED MAXI PAD?
The FDA 510(k) record lists Kimberly-Clark Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KOTEX PROFILE SHAPED MAXI PAD?
The FDA product code for KOTEX PROFILE SHAPED MAXI PAD is HHD.
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 Kimberly-Clark 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: HHD)
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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