REUSABLE MENSTRUAL PAD
K-Number: K924502 · 1994-11-30
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Device Summary
Frequently Asked Questions
What is the REUSABLE MENSTRUAL PAD?
REUSABLE MENSTRUAL PAD is a medical device that received FDA 510(k) clearance on 1994-11-30. The listed applicant is Keema and Co.. The 510(k) number is K924502.
When did REUSABLE MENSTRUAL PAD receive FDA 510(k) clearance?
REUSABLE MENSTRUAL PAD received FDA 510(k) clearance on 1994-11-30, under 510(k) number K924502.
Who is the listed applicant for REUSABLE MENSTRUAL PAD?
The FDA 510(k) record lists Keema and Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REUSABLE MENSTRUAL PAD?
The FDA product code for REUSABLE MENSTRUAL PAD 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.
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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