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DISPOSABLE SUTURE REMOVAL SCISSORS

K812555 Class I Traditional
Decision Date
1981-11-16
Sponsor / Applicant
Medcare Products

Technical Specification

510(k) Submission ID K812555
Product Code JOK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6820
Decision Date 1981-11-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE SUTURE REMOVAL SCISSORS received FDA 510(k) clearance under submission number K812555, sponsored by Medcare Products. 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 1981-11-16.

Classification & Regulation

This clearance is catalogued under FDA product code JOK and 21 CFR 880.6820, within the General Hospital review panel as a Class I device.