WHENEVER UNSCENTED SUPER THIN MAXI-PADS
K-Number: K861356 · 1986-04-23
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Device Summary
Frequently Asked Questions
What is the WHENEVER UNSCENTED SUPER THIN MAXI-PADS?
WHENEVER UNSCENTED SUPER THIN MAXI-PADS is a medical device that received FDA 510(k) clearance on 1986-04-23. The listed applicant is Marcal Paper Mills, Inc.. The 510(k) number is K861356.
When did WHENEVER UNSCENTED SUPER THIN MAXI-PADS receive FDA 510(k) clearance?
WHENEVER UNSCENTED SUPER THIN MAXI-PADS received FDA 510(k) clearance on 1986-04-23, under 510(k) number K861356.
Who is the listed applicant for WHENEVER UNSCENTED SUPER THIN MAXI-PADS?
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 UNSCENTED SUPER THIN MAXI-PADS?
The FDA product code for WHENEVER UNSCENTED SUPER THIN MAXI-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 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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