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FDA 510(k)

CAREFREE * PANTY SHIELDS-REG/DEOR

K-Number: K832382 · 1983-08-12

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1983-08-12
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CAREFREE * PANTY SHIELDS-REG/DEOR is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832382. 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 CAREFREE * PANTY SHIELDS-REG/DEOR?

CAREFREE * PANTY SHIELDS-REG/DEOR is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K832382.

When did CAREFREE * PANTY SHIELDS-REG/DEOR receive FDA 510(k) clearance?

CAREFREE * PANTY SHIELDS-REG/DEOR received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832382.

Who is the listed applicant for CAREFREE * PANTY SHIELDS-REG/DEOR?

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

What is the FDA product code for CAREFREE * PANTY SHIELDS-REG/DEOR?

The FDA product code for CAREFREE * PANTY SHIELDS-REG/DEOR 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.K913238ALWAYS, UNSCENTED MENSTRUAL PADProcter & Gamble Co.K913237ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PADProcter & Gamble Co.

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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