ATTENDS DISPOS. UNDERPAD
K-Number: K853880 · 1985-10-16
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Device Summary
Frequently Asked Questions
What is the ATTENDS DISPOS. UNDERPAD?
ATTENDS DISPOS. UNDERPAD is a medical device that received FDA 510(k) clearance on 1985-10-16. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K853880.
When did ATTENDS DISPOS. UNDERPAD receive FDA 510(k) clearance?
ATTENDS DISPOS. UNDERPAD received FDA 510(k) clearance on 1985-10-16, under 510(k) number K853880.
Who is the listed applicant for ATTENDS DISPOS. UNDERPAD?
The FDA 510(k) record lists Procter & Gamble Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ATTENDS DISPOS. UNDERPAD?
The FDA product code for ATTENDS DISPOS. UNDERPAD is KME.
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 Procter & Gamble Mfg. Co. 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: KME)
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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