meddevicedb.com FDA Device Reference

DRAPES, MODESTY

K770396 Class II Traditional
Decision Date
1977-03-23
Sponsor / Applicant
Mark One Healthcare Products

Technical Specification

510(k) Submission ID K770396
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1977-03-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DRAPES, MODESTY received FDA 510(k) clearance under submission number K770396, sponsored by Mark One Healthcare Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1977-03-23.

Classification & Regulation

This clearance is catalogued under FDA product code KKX and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.