SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS
K-Number: K873457 · 1988-01-19
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Device Summary
Frequently Asked Questions
What is the SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS?
SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K873457.
When did SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS receive FDA 510(k) clearance?
SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS received FDA 510(k) clearance on 1988-01-19, under 510(k) number K873457.
Who is the listed applicant for SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS?
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 SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS?
The FDA product code for SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS is HIL.
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: HIL)
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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