MODIFIED UNSCENTED MENSTRUAL PADS
K-Number: K831707 · 1983-06-16
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Device Summary
Frequently Asked Questions
What is the MODIFIED UNSCENTED MENSTRUAL PADS?
MODIFIED UNSCENTED MENSTRUAL PADS is a medical device that received FDA 510(k) clearance on 1983-06-16. The listed applicant is Personal Products Co.. The 510(k) number is K831707.
When did MODIFIED UNSCENTED MENSTRUAL PADS receive FDA 510(k) clearance?
MODIFIED UNSCENTED MENSTRUAL PADS received FDA 510(k) clearance on 1983-06-16, under 510(k) number K831707.
Who is the listed applicant for MODIFIED UNSCENTED MENSTRUAL PADS?
The FDA 510(k) record lists Personal Products Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFIED UNSCENTED MENSTRUAL PADS?
The FDA product code for MODIFIED UNSCENTED MENSTRUAL PADS is HHD.
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 Personal Products 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: HHD)
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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