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FDA 510(k)

SELF SUPER MAXI SNAITARY NAPKINS

K-Number: K942814 · 1994-08-05

Decision Date1994-08-05
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SELF SUPER MAXI SNAITARY NAPKINS is the device name listed in this FDA 510(k) record. The listed applicant is Kegan & Kegan, Ltd.. It received FDA 510(k) clearance on 1994-08-05 under 510(k) number K942814. 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 SELF SUPER MAXI SNAITARY NAPKINS?

SELF SUPER MAXI SNAITARY NAPKINS is a medical device that received FDA 510(k) clearance on 1994-08-05. The listed applicant is Kegan & Kegan, Ltd.. The 510(k) number is K942814.

When did SELF SUPER MAXI SNAITARY NAPKINS receive FDA 510(k) clearance?

SELF SUPER MAXI SNAITARY NAPKINS received FDA 510(k) clearance on 1994-08-05, under 510(k) number K942814.

Who is the listed applicant for SELF SUPER MAXI SNAITARY NAPKINS?

The FDA 510(k) record lists Kegan & Kegan, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SELF SUPER MAXI SNAITARY NAPKINS?

The FDA product code for SELF SUPER MAXI SNAITARY NAPKINS 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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