ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD
K-Number: K913237 · 1991-09-23
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Device Summary
Frequently Asked Questions
What is the ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD?
ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD is a medical device that received FDA 510(k) clearance on 1991-09-23. The listed applicant is Procter & Gamble Co.. The 510(k) number is K913237.
When did ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD receive FDA 510(k) clearance?
ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD received FDA 510(k) clearance on 1991-09-23, under 510(k) number K913237.
Who is the listed applicant for ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD?
The FDA 510(k) record lists Procter & Gamble Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD?
The FDA product code for ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD 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 Procter & Gamble 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: 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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