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SUPER MAXITHINS BODY-SHAPED MAXI PADS

K842950 Class I Traditional
Decision Date
1984-08-23
Sponsor / Applicant
Tambrands, Inc.

Technical Specification

510(k) Submission ID K842950
Product Code HHD
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5435
Decision Date 1984-08-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUPER MAXITHINS BODY-SHAPED MAXI PADS received FDA 510(k) clearance under submission number K842950, sponsored by Tambrands, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1984-08-23.

Classification & Regulation

This clearance is catalogued under FDA product code HHD and 21 CFR 884.5435, within the Obstetrics/Gynecology review panel as a Class I device.