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PERCUTANEOUS TRIG. FINGER RELEASE KNIFE

K841320 Class I Traditional
Decision Date
1984-04-24
Sponsor / Applicant
Anapach Effort, Inc.

Technical Specification

510(k) Submission ID K841320
Product Code GES
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1984-04-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERCUTANEOUS TRIG. FINGER RELEASE KNIFE received FDA 510(k) clearance under submission number K841320, sponsored by Anapach Effort, 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 1984-04-24.

Classification & Regulation

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