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STANDARD AND EXTENDED BLADE, NEEDLE AND BALL; MODIFIED STANDARD AND EXTENDED BLADE & NEEDLE; STANDARD 45 DEGREE BLADE

K974735 Class II Traditional
Decision Date
1998-06-24
Sponsor / Applicant
Aaron Medical Industries

Technical Specification

510(k) Submission ID K974735
Product Code JOS
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1998-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STANDARD AND EXTENDED BLADE, NEEDLE AND BALL; MODIFIED STANDARD AND EXTENDED BLADE & NEEDLE; STANDARD 45 DEGREE BLADE received FDA 510(k) clearance under submission number K974735, sponsored by Aaron Medical Industries. 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 1998-06-24.

Classification & Regulation

This clearance is catalogued under FDA product code JOS and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.