NEW FREEDOM ANYDAY PANTILINERS
K-Number: K801358 · 1980-07-21
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Device Summary
Frequently Asked Questions
What is the NEW FREEDOM ANYDAY PANTILINERS?
NEW FREEDOM ANYDAY PANTILINERS is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K801358.
When did NEW FREEDOM ANYDAY PANTILINERS receive FDA 510(k) clearance?
NEW FREEDOM ANYDAY PANTILINERS received FDA 510(k) clearance on 1980-07-21, under 510(k) number K801358.
Who is the listed applicant for NEW FREEDOM ANYDAY PANTILINERS?
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 NEW FREEDOM ANYDAY PANTILINERS?
The FDA product code for NEW FREEDOM ANYDAY PANTILINERS is HHL.
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: HHL)
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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