SCENTED ALWAYS PANTILINERS
K-Number: K853000 · 1985-09-06
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Device Summary
Frequently Asked Questions
What is the SCENTED ALWAYS PANTILINERS?
SCENTED ALWAYS PANTILINERS is a medical device that received FDA 510(k) clearance on 1985-09-06. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K853000.
When did SCENTED ALWAYS PANTILINERS receive FDA 510(k) clearance?
SCENTED ALWAYS PANTILINERS received FDA 510(k) clearance on 1985-09-06, under 510(k) number K853000.
Who is the listed applicant for SCENTED ALWAYS PANTILINERS?
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 ALWAYS PANTILINERS?
The FDA product code for SCENTED ALWAYS 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 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: 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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