meddevicedb.com FDA Device Reference

SCISSORS, MAYO _TYLE, 14,16,18,20,22 CM.

K770542 Class I Traditional
Decision Date
1977-04-15
Sponsor / Applicant
Sea-Pac Trading Corp.

Technical Specification

510(k) Submission ID K770542
Product Code FZT
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1977-04-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SCISSORS, MAYO _TYLE, 14,16,18,20,22 CM. received FDA 510(k) clearance under submission number K770542, sponsored by Sea-Pac Trading Corp.. 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 1977-04-15.

Classification & Regulation

This clearance is catalogued under FDA product code FZT and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.