STAYFREE(TM) MAXI-PAD
K-Number: K913747 · 1991-11-05
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Device Summary
Frequently Asked Questions
What is the STAYFREE(TM) MAXI-PAD?
STAYFREE(TM) MAXI-PAD is a medical device that received FDA 510(k) clearance on 1991-11-05. The listed applicant is Personal Products Co.. The 510(k) number is K913747.
When did STAYFREE(TM) MAXI-PAD receive FDA 510(k) clearance?
STAYFREE(TM) MAXI-PAD received FDA 510(k) clearance on 1991-11-05, under 510(k) number K913747.
Who is the listed applicant for STAYFREE(TM) MAXI-PAD?
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 STAYFREE(TM) MAXI-PAD?
The FDA product code for STAYFREE(TM) MAXI-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.
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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