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FDA 510(k)

KAY-PLUS & VARIOUS VANIA SANITARY LINERS & PADS

K-Number: K870066 · 1987-06-19

ApplicantCascades Psh, Inc.
Decision Date1987-06-19
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KAY-PLUS & VARIOUS VANIA SANITARY LINERS & PADS is the device name listed in this FDA 510(k) record. The listed applicant is Cascades Psh, Inc.. It received FDA 510(k) clearance on 1987-06-19 under 510(k) number K870066. The device is classified under product code HHL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAY-PLUS & VARIOUS VANIA SANITARY LINERS & PADS?

KAY-PLUS & VARIOUS VANIA SANITARY LINERS & PADS is a medical device that received FDA 510(k) clearance on 1987-06-19. The listed applicant is Cascades Psh, Inc.. The 510(k) number is K870066.

When did KAY-PLUS & VARIOUS VANIA SANITARY LINERS & PADS receive FDA 510(k) clearance?

KAY-PLUS & VARIOUS VANIA SANITARY LINERS & PADS received FDA 510(k) clearance on 1987-06-19, under 510(k) number K870066.

Who is the listed applicant for KAY-PLUS & VARIOUS VANIA SANITARY LINERS & PADS?

The FDA 510(k) record lists Cascades Psh, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KAY-PLUS & VARIOUS VANIA SANITARY LINERS & PADS?

The FDA product code for KAY-PLUS & VARIOUS VANIA SANITARY LINERS & PADS is HHL.

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Related Devices (Code: HHL)

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.

K962954DEODORANT MAXI PADParagon Trade Brands, Inc.K962953DEODORANT PANTY SHIELDParagon Trade Brands, Inc.K962962DEODORANT PANTY LINERParagon Trade Brands, Inc.K961119CAREFREE PANTYLINERSPersonal Products Co.K913237ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PADProcter & Gamble Co.K913238ALWAYS, UNSCENTED MENSTRUAL PADProcter & Gamble Co.

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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