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TRAY, SUTURE REMOVAL

K760051 Class I Traditional
Decision Date
1976-08-30
Sponsor / Applicant
M-C Ind., Inc.

Technical Specification

510(k) Submission ID K760051
Product Code KDD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1976-08-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRAY, SUTURE REMOVAL received FDA 510(k) clearance under submission number K760051, sponsored by M-C Ind., Inc.. 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 1976-08-30.

Classification & Regulation

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