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PRISMA TECH 19 GAUGE DISPOSABLE EXTRUSION NEEDLES

K881927 Class II Traditional
Decision Date
1988-05-25
Sponsor / Applicant
Advanced Surgical Products, Inc.

Technical Specification

510(k) Submission ID K881927
Product Code HQE
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4150
Decision Date 1988-05-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRISMA TECH 19 GAUGE DISPOSABLE EXTRUSION NEEDLES received FDA 510(k) clearance under submission number K881927, sponsored by Advanced Surgical Products, 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 1988-05-25.

Classification & Regulation

This clearance is catalogued under FDA product code HQE and 21 CFR 886.4150, within the Ophthalmic review panel as a Class II device.