meddevicedb.com FDA Device Reference

SKIN CLOSURE

K840945 Class I Traditional
Decision Date
1984-10-31
Sponsor / Applicant
Gainor Medical

Technical Specification

510(k) Submission ID K840945
Product Code FPX
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5240
Decision Date 1984-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SKIN CLOSURE received FDA 510(k) clearance under submission number K840945, sponsored by Gainor Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1984-10-31.

Classification & Regulation

This clearance is catalogued under FDA product code FPX and 21 CFR 880.5240, within the General Hospital review panel as a Class I device.