meddevicedb.com FDA Device Reference

PREGNANCY (W) EDGE

K821836 Class I Traditional
Decision Date
1982-07-30
Sponsor / Applicant
Body Therapeutics, Inc.

Technical Specification

510(k) Submission ID K821836
Product Code QSB
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3490
Decision Date 1982-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PREGNANCY (W) EDGE received FDA 510(k) clearance under submission number K821836, sponsored by Body Therapeutics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1982-07-30.

Classification & Regulation

This clearance is catalogued under FDA product code QSB and 21 CFR 890.3490, within the Physical Medicine review panel as a Class I device.