UNSCENTED CURVED MAXI PAD
K-Number: K953700 · 1995-09-27
Advertisement
Device Summary
Frequently Asked Questions
What is the UNSCENTED CURVED MAXI PAD?
UNSCENTED CURVED MAXI PAD is a medical device that received FDA 510(k) clearance on 1995-09-27. The listed applicant is Paragon Trade Brands, Inc.. The 510(k) number is K953700.
When did UNSCENTED CURVED MAXI PAD receive FDA 510(k) clearance?
UNSCENTED CURVED MAXI PAD received FDA 510(k) clearance on 1995-09-27, under 510(k) number K953700.
Who is the listed applicant for UNSCENTED CURVED MAXI PAD?
The FDA 510(k) record lists Paragon Trade Brands, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNSCENTED CURVED MAXI PAD?
The FDA product code for UNSCENTED CURVED 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 Paragon Trade Brands, 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.
Advertisement