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FDA 510(k)

SCENTED MENSTRUAL PAD

K-Number: K832215 · 1983-07-12

ApplicantPersonal Products Co.
Decision Date1983-07-12
Product Code
DecisionSubstantially Equivalent

Device Summary

SCENTED MENSTRUAL PAD is the device name listed in this FDA 510(k) record. The listed applicant is Personal Products Co.. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K832215. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCENTED MENSTRUAL PAD?

SCENTED MENSTRUAL PAD is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Personal Products Co.. The 510(k) number is K832215.

When did SCENTED MENSTRUAL PAD receive FDA 510(k) clearance?

SCENTED MENSTRUAL PAD received FDA 510(k) clearance on 1983-07-12, under 510(k) number K832215.

Who is the listed applicant for SCENTED MENSTRUAL PAD?

The FDA 510(k) record lists Personal Products Co. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Personal Products Co. as applicant

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.

K070545K-Y BRAND WARMING LIQUIDK062796K-Y BRAND INTRIGUEK010365ORTHO CONTROL FEMALE URINARY CONTROL DEVICEK990536O.B. TAMPONK991118O.B. APPLICATOR TAMPONS, O.B. TAMPONSK974629O.B. APPLICATOR AND NON-APPLICATOR TAMPONS

View all 45 devices →

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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