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FDA 510(k)

NEW FREEDOM ULTRA THIN PADS

K-Number: K920830 · 1992-09-04

Decision Date1992-09-04
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NEW FREEDOM ULTRA THIN PADS is the device name listed in this FDA 510(k) record. The listed applicant is Kimberly-Clark Corp.. It received FDA 510(k) clearance on 1992-09-04 under 510(k) number K920830. The device is classified under product code HHD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW FREEDOM ULTRA THIN PADS?

NEW FREEDOM ULTRA THIN PADS is a medical device that received FDA 510(k) clearance on 1992-09-04. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K920830.

When did NEW FREEDOM ULTRA THIN PADS receive FDA 510(k) clearance?

NEW FREEDOM ULTRA THIN PADS received FDA 510(k) clearance on 1992-09-04, under 510(k) number K920830.

Who is the listed applicant for NEW FREEDOM ULTRA THIN PADS?

The FDA 510(k) record lists Kimberly-Clark Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEW FREEDOM ULTRA THIN PADS?

The FDA product code for NEW FREEDOM ULTRA THIN 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 Kimberly-Clark Corp. 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.

View all 102 devices →

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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