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SURGICAL SPEARS

K923922 Class II Traditional
Decision Date
1993-03-19
Sponsor / Applicant
Ultracell Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K923922
Product Code HOZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4790
Decision Date 1993-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL SPEARS received FDA 510(k) clearance under submission number K923922, sponsored by Ultracell Medical Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1993-03-19.

Classification & Regulation

This clearance is catalogued under FDA product code HOZ and 21 CFR 886.4790, within the Ophthalmic review panel as a Class II device.