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FDA 510(k)

KOTEX SUPER MAXI PADS

K-Number: K890013 · 1989-04-25

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

Device Summary

KOTEX SUPER MAXI 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 1989-04-25 under 510(k) number K890013. The device is classified under product code HHT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOTEX SUPER MAXI PADS?

KOTEX SUPER MAXI PADS 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 K890013.

When did KOTEX SUPER MAXI PADS receive FDA 510(k) clearance?

KOTEX SUPER MAXI PADS received FDA 510(k) clearance on 1989-04-25, under 510(k) number K890013.

Who is the listed applicant for KOTEX SUPER MAXI 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 KOTEX SUPER MAXI PADS?

The FDA product code for KOTEX SUPER MAXI PADS is HHT.

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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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