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FDA 510(k)

FEMININE HYGIENE DEVICE

K-Number: K831667 · 1983-09-12

ApplicantSnow Willow Co.
Decision Date1983-09-12
Product CodeHED
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FEMININE HYGIENE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Snow Willow Co.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K831667. The device is classified under product code HED. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEMININE HYGIENE DEVICE?

FEMININE HYGIENE DEVICE is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Snow Willow Co.. The 510(k) number is K831667.

When did FEMININE HYGIENE DEVICE receive FDA 510(k) clearance?

FEMININE HYGIENE DEVICE received FDA 510(k) clearance on 1983-09-12, under 510(k) number K831667.

Who is the listed applicant for FEMININE HYGIENE DEVICE?

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

What is the FDA product code for FEMININE HYGIENE DEVICE?

The FDA product code for FEMININE HYGIENE DEVICE is HED.

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Related Devices (Code: HED)

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.

K080200WATER WORKS DOUCHING DEVICEAbbott Research Group, Inc.K030056WORRY-REMOVER IRRIGATORCorisen Group, Ltd.K000736LA JOIEGoomi Ehwa, Inc.K902830PERI-BOTTLEOrion Life Systems, Inc.K881216GENT-L-KARE VAGINAL IRRIGATION SETGeneva Laboratories, Inc.K854595P.A. MEDICAL VAGINAL IRRIGATION SET #1130Pa Medical Corp.

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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