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FDA 510(k)

NEW FREEDOM THIN SUPER & UNSCENTED, MAXI & SUPER

K-Number: K890654 · 1989-04-25

ApplicantKimberly-Clark Corp.
Decision Date1989-04-25
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NEW FREEDOM THIN SUPER & UNSCENTED, MAXI & SUPER 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 1989-04-25 under 510(k) number K890654. 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 THIN SUPER & UNSCENTED, MAXI & SUPER?

NEW FREEDOM THIN SUPER & UNSCENTED, MAXI & SUPER is a medical device that received FDA 510(k) clearance on 1989-04-25. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K890654.

When did NEW FREEDOM THIN SUPER & UNSCENTED, MAXI & SUPER receive FDA 510(k) clearance?

NEW FREEDOM THIN SUPER & UNSCENTED, MAXI & SUPER received FDA 510(k) clearance on 1989-04-25, under 510(k) number K890654.

Who is the listed applicant for NEW FREEDOM THIN SUPER & UNSCENTED, MAXI & SUPER?

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 THIN SUPER & UNSCENTED, MAXI & SUPER?

The FDA product code for NEW FREEDOM THIN SUPER & UNSCENTED, MAXI & SUPER is HHD.

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Other records listing Kimberly-Clark Corp. as applicant

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Related Devices (Code: HHD)

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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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