WHENEVER(R) UNSCENTED SUPER MAXI PAD
K-Number: K901690 · 1990-08-21
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Device Summary
Frequently Asked Questions
What is the WHENEVER(R) UNSCENTED SUPER MAXI PAD?
WHENEVER(R) UNSCENTED SUPER MAXI PAD is a medical device that received FDA 510(k) clearance on 1990-08-21. The listed applicant is Marcal Paper Mills, Inc.. The 510(k) number is K901690.
When did WHENEVER(R) UNSCENTED SUPER MAXI PAD receive FDA 510(k) clearance?
WHENEVER(R) UNSCENTED SUPER MAXI PAD received FDA 510(k) clearance on 1990-08-21, under 510(k) number K901690.
Who is the listed applicant for WHENEVER(R) UNSCENTED SUPER MAXI PAD?
The FDA 510(k) record lists Marcal Paper Mills, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WHENEVER(R) UNSCENTED SUPER MAXI PAD?
The FDA product code for WHENEVER(R) UNSCENTED SUPER 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 Marcal Paper Mills, Inc. 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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